Canonical Allele Identifier: CA1826365558
Gene: RECQL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144512038A= , CM000670.2:g.144512038A= GRCh38
NC_000008.10:g.145737421A= , CM000670.1:g.145737421A= GRCh37
NC_000008.9:g.145708229A= NCBI36
NG_016430.1:g.10789T=
NG_016430.2:g.10789T=

Transcript Alleles

HGVS Amino-acid change
ENST00000617875.6:c.3266T= MANE Select ENSP00000482313.2:p.Leu1089=
ENST00000301323.7:c.283T=
ENST00000529424.2:n.50-249T=
ENST00000531875.2:c.512T= ENSP00000477910.1:p.Leu171=
ENST00000617875.4:c.3266T= ENSP00000482313.1:p.Leu1089=
ENST00000621189.4:c.2195T= ENSP00000483145.1:p.Leu732=
NM_004260.3:c.3266T= NP_004251.3:p.Leu1089=
XM_011517380.1:c.3341T= XP_011515682.1:p.Leu1114=
XM_011517381.1:c.3245T= XP_011515683.1:p.Leu1082=
XM_011517382.1:c.3149T= XP_011515684.1:p.Leu1050=
XM_011517383.1:c.3143T= XP_011515685.1:p.Leu1048=
XM_011517384.1:c.3068T= XP_011515686.1:p.Leu1023=
XM_011517385.1:c.2204T= XP_011515687.1:p.Leu735=
XR_928366.1:n.3352+106T=
XR_928367.1:n.3321T=
XR_928368.1:n.3214T=
XM_011517384.3:c.3068T= XP_011515686.1:p.Leu1023=
XM_017013991.2:c.3431T= XP_016869480.1:p.Leu1144=
XM_017013992.2:c.3356T= XP_016869481.1:p.Leu1119=
XM_017013993.2:c.3341T= XP_016869482.1:p.Leu1114=
XM_017013994.2:c.3335T= XP_016869483.1:p.Leu1112=
XM_017013995.2:c.3266T= XP_016869484.1:p.Leu1089=
XM_017013996.2:c.3431T= XP_016869485.1:p.Leu1144=
XM_017013997.2:c.3233T= XP_016869486.1:p.Leu1078=
XM_017013998.1:c.3356T= XP_016869487.1:p.Leu1119=
XM_017013999.2:c.3143T= XP_016869488.1:p.Leu1048=
XM_017014000.1:c.2294T= XP_016869489.1:p.Leu765=
XM_017014001.2:c.2204T= XP_016869490.1:p.Leu735=
XR_001745626.2:n.3438+106T=
XR_001745627.2:n.3407T=
XR_001745628.2:n.3298T=
XR_001745629.2:n.3161T=
XR_001745630.2:n.2963T=
NM_004260.4:c.3266T= MANE Select NP_004251.4:p.Leu1089=