Canonical Allele Identifier: CA337728961
Gene: UTY HGNC NCBI

Linked Data

dbSNP Id: rs16980601

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13303235A>G , CM000686.2:g.13303235A>G GRCh38
NC_000024.9:g.15415115A>G , CM000686.1:g.15415115A>G GRCh37
NC_000024.8:g.13924509A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000331397.8:c.3275-244T>C ENSP00000328939.4:p.=
ENST00000362096.8:c.3275-244T>C ENSP00000355420.4:p.=
ENST00000382896.8:c.3410-244T>C ENSP00000372352.4:p.=
ENST00000537580.5:c.3410-244T>C ENSP00000439922.2:p.=
ENST00000538878.5:c.3323-244T>C ENSP00000445274.2:p.=
ENST00000540140.5:c.3401-244T>C ENSP00000441943.2:p.=
ENST00000545955.5:c.3566-244T>C ENSP00000442047.2:p.=
ENST00000612274.4:c.3335-244T>C ENSP00000485013.1:p.=
ENST00000617789.4:c.3431-244T>C ENSP00000483735.1:p.=
ENST00000618474.4:c.3026-244T>C ENSP00000484698.1:p.=
ENST00000624098.3:n.3038-244T>C ENSP00000485539.2:p.=
NM_001258249.1:c.3566-244T>C NP_001245178.1:p.=
NM_001258250.1:c.2855-244T>C NP_001245179.1:p.=
NM_001258251.1:c.3323-244T>C NP_001245180.1:p.=
NM_001258252.1:c.3410-244T>C NP_001245181.1:p.=
NM_001258253.1:c.3323-244T>C NP_001245182.1:p.=
NM_001258254.1:c.3038-244T>C NP_001245183.1:p.=
NM_001258255.1:c.3038-244T>C NP_001245184.1:p.=
NM_001258256.1:c.3410-244T>C NP_001245185.1:p.=
NM_001258257.1:c.2903-244T>C NP_001245186.1:p.=
NM_001258258.1:c.3431-244T>C NP_001245187.1:p.=
NM_001258259.1:c.3227-244T>C NP_001245188.1:p.=
NM_001258260.1:c.3365-244T>C NP_001245189.1:p.=
NM_001258261.1:c.3401-244T>C NP_001245190.1:p.=
NM_001258262.1:c.3194-244T>C NP_001245191.1:p.=
NM_001258263.1:c.3275-244T>C NP_001245192.1:p.=
NM_001258264.1:c.3362-244T>C NP_001245193.1:p.=
NM_001258265.1:c.3026-244T>C NP_001245194.1:p.=
NM_001258266.1:c.3335-244T>C NP_001245195.1:p.=
NM_001258267.1:c.3275-244T>C NP_001245196.1:p.=
NM_001258268.1:c.3038-244T>C NP_001245197.1:p.=
NM_001258269.1:c.3128-244T>C NP_001245198.1:p.=
NM_001258270.1:c.2903-244T>C NP_001245199.1:p.=
NM_007125.4:c.3275-244T>C NP_009056.3:p.=
NM_182659.1:c.3275-244T>C NP_872600.1:p.=
NR_047596.1:n.3507-244T>C
NR_047597.1:n.4386-244T>C
NR_047598.1:n.4584-244T>C
NR_047599.1:n.4403-244T>C
NR_047600.1:n.4204-244T>C
NR_047601.1:n.3880-244T>C
NR_047602.1:n.4245-244T>C
NR_047603.1:n.4403-244T>C
NR_047604.1:n.3373-244T>C
NR_047605.1:n.3459-244T>C
NR_047606.1:n.3643-244T>C
NR_047607.1:n.4626-244T>C
NR_047608.1:n.3662-244T>C
NR_047609.1:n.4038-244T>C
NR_047610.1:n.3575-244T>C
NR_047611.1:n.3642-244T>C
NR_047612.1:n.3798-244T>C
NR_047613.1:n.3748-244T>C
NR_047614.1:n.3711-244T>C
NR_047615.1:n.3565-244T>C
NR_047616.1:n.3559-244T>C
NR_047617.1:n.3676-244T>C
NR_047618.1:n.4289-244T>C
NR_047619.1:n.3565-244T>C
NR_047620.1:n.3642-244T>C
NR_047621.1:n.3747-244T>C
NR_047622.1:n.3699-244T>C
NR_047623.1:n.3642-244T>C
NR_047624.1:n.4500-244T>C
NR_047625.1:n.3380-244T>C
NR_047626.1:n.3507-244T>C
NR_047627.1:n.3710-244T>C
NR_047628.1:n.3555-244T>C
NR_047629.1:n.3774-244T>C
NR_047630.1:n.3432-244T>C
NR_047631.1:n.3507-244T>C
NR_047632.1:n.3988-244T>C
NR_047633.1:n.3556-244T>C
NR_047634.1:n.3506-244T>C
NR_047635.1:n.4275-244T>C
NR_047636.1:n.3645-244T>C
NR_047637.1:n.4338-244T>C
NR_047638.1:n.4346-244T>C
NR_047639.1:n.3413-244T>C
NR_047640.1:n.3491-244T>C
NR_047641.1:n.4348-244T>C
NR_047642.1:n.4280-244T>C
NR_047643.1:n.3880-244T>C
NR_047644.1:n.4473-244T>C
NR_047645.1:n.4486-244T>C
NR_047646.1:n.4153-244T>C
NR_047647.1:n.4237-244T>C
XM_005262518.2:c.3410-244T>C XP_005262575.1:p.=
XM_006724875.2:c.3566-244T>C XP_006724938.1:p.=
XM_006724876.2:c.3275-244T>C XP_006724939.1:p.=
XM_011531441.1:c.3614-244T>C XP_011529743.1:p.=
XM_011531442.1:c.3566-244T>C XP_011529744.1:p.=
XM_011531443.1:c.3548-244T>C XP_011529745.1:p.=
XM_011531444.1:c.3500-244T>C XP_011529746.1:p.=
XM_011531445.1:c.3479-244T>C XP_011529747.1:p.=
XM_011531446.1:c.3458-244T>C XP_011529748.1:p.=
XM_011531447.1:c.3431-244T>C XP_011529749.1:p.=
XM_011531448.1:c.3413-244T>C XP_011529750.1:p.=
XM_011531449.1:c.3410-244T>C XP_011529751.1:p.=
XM_011531450.1:c.3365-244T>C XP_011529752.1:p.=
XM_011531451.1:c.3323-244T>C XP_011529753.1:p.=
XM_011531452.1:c.3275-244T>C XP_011529754.1:p.=
XM_011531453.1:c.3614-244T>C XP_011529755.1:p.=
XM_011531454.1:c.3614-244T>C XP_011529756.1:p.=
XM_011531455.1:c.3614-244T>C XP_011529757.1:p.=
XM_011531456.1:c.3614-244T>C XP_011529758.1:p.=
XM_011531457.1:c.3614-244T>C XP_011529759.1:p.=
XM_011531458.1:c.3500-244T>C XP_011529760.1:p.=
XM_011531459.1:c.3614-244T>C XP_011529761.1:p.=
XM_011531466.1:c.3548-244T>C XP_011529768.1:p.=
XM_011531467.1:c.3458-244T>C XP_011529769.1:p.=
XM_005262518.4:c.3410-244T>C XP_005262575.1:p.=
XM_006724875.4:c.3566-244T>C XP_006724938.1:p.=
XM_011531441.3:c.3614-244T>C XP_011529743.1:p.=
XM_011531442.3:c.3566-244T>C XP_011529744.1:p.=
XM_011531443.3:c.3548-244T>C XP_011529745.1:p.=
XM_011531445.3:c.3479-244T>C XP_011529747.1:p.=
XM_011531446.3:c.3458-244T>C XP_011529748.1:p.=
XM_011531447.3:c.3431-244T>C XP_011529749.1:p.=
XM_011531448.3:c.3413-244T>C XP_011529750.1:p.=
XM_011531449.3:c.3410-244T>C XP_011529751.1:p.=
XM_011531450.3:c.3365-244T>C XP_011529752.1:p.=
XM_011531451.3:c.3323-244T>C XP_011529753.1:p.=
XM_011531452.3:c.3275-244T>C XP_011529754.1:p.=
XM_011531453.3:c.3614-244T>C XP_011529755.1:p.=
XM_011531454.3:c.3614-244T>C XP_011529756.1:p.=
XM_011531455.3:c.3614-244T>C XP_011529757.1:p.=
XM_011531458.3:c.3500-244T>C XP_011529760.1:p.=
XM_011531459.3:c.3614-244T>C XP_011529761.1:p.=
XM_017030066.2:c.3500-244T>C XP_016885555.1:p.=
XM_017030067.2:c.3410-244T>C XP_016885556.1:p.=
XM_017030068.2:c.3275-244T>C XP_016885557.1:p.=
XM_017030070.2:c.3614-244T>C XP_016885559.1:p.=
XM_017030074.2:c.3548-244T>C XP_016885563.1:p.=
XM_024452493.1:c.3614-244T>C XP_024308261.1:p.=
XR_001756008.2:n.3630-244T>C
XR_002958831.1:n.3013-244T>C
NM_001258249.2:c.3566-244T>C MANE Select NP_001245178.1:p.=