Canonical Allele Identifier: CA369168110
Gene: IMPDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128398448A>G , CM000669.2:g.128398448A>G GRCh38
NC_000007.13:g.128038502A>G , CM000669.1:g.128038502A>G GRCh37
NC_000007.12:g.127825738A>G NCBI36
NG_009194.1:g.16535T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000348127.11:c.932T>C ENSP00000265385.8:p.Leu311Pro
ENST00000484496.6:n.915T>C
ENST00000338791.11:c.1040T>C MANE Select ENSP00000345096.6:p.Leu347Pro
ENST00000648462.1:c.672T>C
ENST00000338791.10:c.1040T>C ENSP00000345096.6:p.Leu347Pro
ENST00000348127.10:c.932T>C ENSP00000265385.8:p.Leu311Pro
ENST00000354269.9:c.1010T>C ENSP00000346219.5:p.Leu337Pro
ENST00000419067.6:c.941T>C ENSP00000399400.2:p.Leu314Pro
ENST00000469328.5:c.805T>C
ENST00000470772.5:c.782T>C ENSP00000417296.1:p.Leu261Pro
ENST00000480861.5:c.770T>C ENSP00000420185.1:p.Leu257Pro
ENST00000484496.5:c.915T>C ENSP00000418742.1:n.915T>C
ENST00000496200.5:c.710T>C ENSP00000420803.1:p.Leu237Pro
ENST00000497868.5:c.833T>C ENSP00000419609.1:p.Leu278Pro
ENST00000626419.2:c.782T>C ENSP00000486056.1:p.Leu261Pro
NM_000883.3:c.1040T>C NP_000874.2:p.Leu347Pro
NM_001102605.1:c.1010T>C NP_001096075.1:p.Leu337Pro
NM_001142573.1:c.785T>C NP_001136045.1:p.Leu262Pro
NM_001142574.1:c.770T>C NP_001136046.1:p.Leu257Pro
NM_001142575.1:c.710T>C NP_001136047.1:p.Leu237Pro
NM_001142576.1:c.941T>C NP_001136048.1:p.Leu314Pro
NM_001304521.1:c.833T>C NP_001291450.1:p.Leu278Pro
NM_183243.2:c.932T>C NP_899066.1:p.Leu311Pro
XM_005250314.1:c.809T>C XP_005250371.1:p.Leu270Pro
XM_006715967.1:c.1040T>C XP_006716030.1:p.Leu347Pro
XM_006715968.1:c.1010T>C XP_006716031.1:p.Leu337Pro
XM_006715969.1:c.932T>C XP_006716032.1:p.Leu311Pro
XM_006715970.2:c.833T>C XP_006716033.1:p.Leu278Pro
XM_006715971.1:c.809T>C XP_006716034.1:p.Leu270Pro
XM_011516156.1:c.422T>C XP_011514458.1:p.Leu141Pro
XM_011516157.1:c.422T>C XP_011514459.1:p.Leu141Pro
XM_017012172.1:c.809T>C XP_016867661.1:p.Leu270Pro
XM_017012173.1:c.1010T>C XP_016867662.1:p.Leu337Pro
XM_024446755.1:c.1010T>C XP_024302523.1:p.Leu337Pro
XM_024446756.1:c.932T>C XP_024302524.1:p.Leu311Pro
XM_024446757.1:c.833T>C XP_024302525.1:p.Leu278Pro
XM_024446758.1:c.809T>C XP_024302526.1:p.Leu270Pro
NM_000883.4:c.1040T>C MANE Select NP_000874.2:p.Leu347Pro
NM_001102605.2:c.1010T>C NP_001096075.1:p.Leu337Pro
NM_001142573.2:c.785T>C NP_001136045.1:p.Leu262Pro
NM_001142574.2:c.770T>C NP_001136046.1:p.Leu257Pro
NM_001142575.2:c.710T>C NP_001136047.1:p.Leu237Pro
NM_001142576.2:c.941T>C NP_001136048.1:p.Leu314Pro
NM_001304521.2:c.833T>C NP_001291450.1:p.Leu278Pro
NM_183243.3:c.932T>C NP_899066.1:p.Leu311Pro