Canonical Allele Identifier: CA2504873424
Gene: IMPDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128398639G>C , CM000669.2:g.128398639G>C GRCh38
NC_000007.13:g.128038693G>C , CM000669.1:g.128038693G>C GRCh37
NC_000007.12:g.127825929G>C NCBI36
NG_009194.1:g.16344C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000348127.11:c.767-26C>G ENSP00000265385.8:n.767-26C>G
ENST00000484496.6:n.750-26C>G
ENST00000338791.11:c.875-26C>G MANE Select ENSP00000345096.6:n.875-26C>G
ENST00000648462.1:c.507-26C>G
ENST00000338791.10:c.875-26C>G ENSP00000345096.6:n.875-26C>G
ENST00000348127.10:c.767-26C>G ENSP00000265385.8:n.767-26C>G
ENST00000354269.9:c.845-26C>G ENSP00000346219.5:n.845-26C>G
ENST00000419067.6:c.776-26C>G ENSP00000399400.2:n.776-26C>G
ENST00000468842.1:n.464-26C>G
ENST00000469328.5:c.640-26C>G
ENST00000470772.5:c.617-26C>G ENSP00000417296.1:n.617-26C>G
ENST00000480861.5:c.605-26C>G ENSP00000420185.1:n.605-26C>G
ENST00000484496.5:c.750-26C>G ENSP00000418742.1:n.750-26C>G
ENST00000496200.5:c.545-26C>G ENSP00000420803.1:n.545-26C>G
ENST00000497868.5:c.668-26C>G ENSP00000419609.1:n.668-26C>G
ENST00000626419.2:c.617-26C>G ENSP00000486056.1:n.617-26C>G
NM_000883.3:c.875-26C>G NP_000874.2:n.875-26C>G
NM_001102605.1:c.845-26C>G NP_001096075.1:n.845-26C>G
NM_001142573.1:c.620-26C>G NP_001136045.1:n.620-26C>G
NM_001142574.1:c.605-26C>G NP_001136046.1:n.605-26C>G
NM_001142575.1:c.545-26C>G NP_001136047.1:n.545-26C>G
NM_001142576.1:c.776-26C>G NP_001136048.1:n.776-26C>G
NM_001304521.1:c.668-26C>G NP_001291450.1:n.668-26C>G
NM_183243.2:c.767-26C>G NP_899066.1:n.767-26C>G
XM_005250314.1:c.644-26C>G XP_005250371.1:n.644-26C>G
XM_006715967.1:c.875-26C>G XP_006716030.1:n.875-26C>G
XM_006715968.1:c.845-26C>G XP_006716031.1:n.845-26C>G
XM_006715969.1:c.767-26C>G XP_006716032.1:n.767-26C>G
XM_006715970.2:c.668-26C>G XP_006716033.1:n.668-26C>G
XM_006715971.1:c.644-26C>G XP_006716034.1:n.644-26C>G
XM_011516156.1:c.257-26C>G XP_011514458.1:n.257-26C>G
XM_011516157.1:c.257-26C>G XP_011514459.1:n.257-26C>G
XM_017012172.1:c.644-26C>G XP_016867661.1:n.644-26C>G
XM_017012173.1:c.845-26C>G XP_016867662.1:n.845-26C>G
XM_024446755.1:c.845-26C>G XP_024302523.1:n.845-26C>G
XM_024446756.1:c.767-26C>G XP_024302524.1:n.767-26C>G
XM_024446757.1:c.668-26C>G XP_024302525.1:n.668-26C>G
XM_024446758.1:c.644-26C>G XP_024302526.1:n.644-26C>G
NM_000883.4:c.875-26C>G MANE Select NP_000874.2:n.875-26C>G
NM_001102605.2:c.845-26C>G NP_001096075.1:n.845-26C>G
NM_001142573.2:c.620-26C>G NP_001136045.1:n.620-26C>G
NM_001142574.2:c.605-26C>G NP_001136046.1:n.605-26C>G
NM_001142575.2:c.545-26C>G NP_001136047.1:n.545-26C>G
NM_001142576.2:c.776-26C>G NP_001136048.1:n.776-26C>G
NM_001304521.2:c.668-26C>G NP_001291450.1:n.668-26C>G
NM_183243.3:c.767-26C>G NP_899066.1:n.767-26C>G