Canonical Allele Identifier: CA369174419
Gene: IMPDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128401047C>G , CM000669.2:g.128401047C>G GRCh38
NC_000007.13:g.128041101C>G , CM000669.1:g.128041101C>G GRCh37
NC_000007.12:g.127828337C>G NCBI36
NG_009194.1:g.13936G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000348127.11:c.364G>C ENSP00000265385.8:p.Val122Leu
ENST00000484496.6:n.328G>C
ENST00000338791.11:c.472G>C MANE Select ENSP00000345096.6:p.Val158Leu
ENST00000648462.1:c.119G>C
ENST00000338791.10:c.472G>C ENSP00000345096.6:p.Val158Leu
ENST00000348127.10:c.364G>C ENSP00000265385.8:p.Val122Leu
ENST00000354269.9:c.442G>C ENSP00000346219.5:p.Val148Leu
ENST00000419067.6:c.373G>C ENSP00000399400.2:p.Val125Leu
ENST00000469328.5:c.218G>C
ENST00000470772.5:c.217G>C ENSP00000417296.1:p.Val73Leu
ENST00000473463.1:c.*218G>C ENSP00000420469.1:n.*218G>C
ENST00000480861.5:c.217G>C ENSP00000420185.1:p.Val73Leu
ENST00000484496.5:c.328G>C ENSP00000418742.1:p.Val110Leu
ENST00000489263.1:c.265G>C ENSP00000418592.1:p.Val89Leu
ENST00000491376.5:n.641G>C
ENST00000496200.5:c.217G>C ENSP00000420803.1:p.Val73Leu
ENST00000496487.5:n.292G>C
ENST00000497868.5:c.265G>C ENSP00000419609.1:p.Val89Leu
ENST00000626419.2:c.217G>C ENSP00000486056.1:p.Val73Leu
NM_000883.3:c.472G>C NP_000874.2:p.Val158Leu
NM_001102605.1:c.442G>C NP_001096075.1:p.Val148Leu
NM_001142573.1:c.217G>C NP_001136045.1:p.Val73Leu
NM_001142574.1:c.217G>C NP_001136046.1:p.Val73Leu
NM_001142575.1:c.217G>C NP_001136047.1:p.Val73Leu
NM_001142576.1:c.373G>C NP_001136048.1:p.Val125Leu
NM_001304521.1:c.265G>C NP_001291450.1:p.Val89Leu
NM_183243.2:c.364G>C NP_899066.1:p.Val122Leu
XM_005250314.1:c.241G>C XP_005250371.1:p.Val81Leu
XM_006715967.1:c.472G>C XP_006716030.1:p.Val158Leu
XM_006715968.1:c.442G>C XP_006716031.1:p.Val148Leu
XM_006715969.1:c.364G>C XP_006716032.1:p.Val122Leu
XM_006715970.2:c.265G>C XP_006716033.1:p.Val89Leu
XM_006715971.1:c.241G>C XP_006716034.1:p.Val81Leu
XM_017012172.1:c.241G>C XP_016867661.1:p.Val81Leu
XM_017012173.1:c.442G>C XP_016867662.1:p.Val148Leu
XM_024446755.1:c.442G>C XP_024302523.1:p.Val148Leu
XM_024446756.1:c.364G>C XP_024302524.1:p.Val122Leu
XM_024446757.1:c.265G>C XP_024302525.1:p.Val89Leu
XM_024446758.1:c.241G>C XP_024302526.1:p.Val81Leu
NM_000883.4:c.472G>C MANE Select NP_000874.2:p.Val158Leu
NM_001102605.2:c.442G>C NP_001096075.1:p.Val148Leu
NM_001142573.2:c.217G>C NP_001136045.1:p.Val73Leu
NM_001142574.2:c.217G>C NP_001136046.1:p.Val73Leu
NM_001142575.2:c.217G>C NP_001136047.1:p.Val73Leu
NM_001142576.2:c.373G>C NP_001136048.1:p.Val125Leu
NM_001304521.2:c.265G>C NP_001291450.1:p.Val89Leu
NM_183243.3:c.364G>C NP_899066.1:p.Val122Leu