Canonical Allele Identifier: CA4470898

Gene: IMPDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128396635C>T , CM000669.2:g.128396635C>T	GRCh38
NC_000007.13:g.128036689C>T , CM000669.1:g.128036689C>T	GRCh37
NC_000007.12:g.127823925C>T	NCBI36
NG_009194.1:g.18348G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000883.4:c.1226G>A MANE Select	NP_000874.2:p.Gly409Asp
ENST00000338791.11:c.1226G>A MANE Select	ENSP00000345096.6:p.Gly409Asp
NM_000883.3:c.1226G>A	NP_000874.2:p.Gly409Asp
NM_001102605.1:c.1196G>A	NP_001096075.1:p.Gly399Asp
NM_001102605.2:c.1196G>A	NP_001096075.1:p.Gly399Asp
NM_001142573.1:c.971G>A	NP_001136045.1:p.Gly324Asp
NM_001142573.2:c.971G>A	NP_001136045.1:p.Gly324Asp
NM_001142574.1:c.956G>A	NP_001136046.1:p.Gly319Asp
NM_001142574.2:c.956G>A	NP_001136046.1:p.Gly319Asp
NM_001142575.1:c.896G>A	NP_001136047.1:p.Gly299Asp
NM_001142575.2:c.896G>A	NP_001136047.1:p.Gly299Asp
NM_001142576.1:c.1127G>A	NP_001136048.1:p.Gly376Asp
NM_001142576.2:c.1127G>A	NP_001136048.1:p.Gly376Asp
NM_001304521.1:c.1019G>A	NP_001291450.1:p.Gly340Asp
NM_001304521.2:c.1019G>A	NP_001291450.1:p.Gly340Asp
NM_183243.2:c.1118G>A	NP_899066.1:p.Gly373Asp
NM_183243.3:c.1118G>A	NP_899066.1:p.Gly373Asp
ENST00000338791.10:c.1226G>A	ENSP00000345096.6:p.Gly409Asp
ENST00000348127.10:c.1118G>A	ENSP00000265385.8:p.Gly373Asp
ENST00000348127.11:c.1118G>A	ENSP00000265385.8:p.Gly373Asp
ENST00000354269.9:c.1196G>A	ENSP00000346219.5:p.Gly399Asp
ENST00000419067.6:c.1127G>A	ENSP00000399400.2:p.Gly376Asp
ENST00000469328.5:c.991G>A
ENST00000470772.5:c.968G>A	ENSP00000417296.1:p.Gly323Asp
ENST00000480861.5:c.956G>A	ENSP00000420185.1:p.Gly319Asp
ENST00000484496.5:c.1101G>A	ENSP00000418742.1:n.1101G>A
ENST00000484496.6:n.1101G>A
ENST00000496200.5:c.896G>A	ENSP00000420803.1:p.Gly299Asp
ENST00000626419.2:c.968G>A	ENSP00000486056.1:p.Gly323Asp
ENST00000648462.1:c.858G>A
XM_005250314.1:c.995G>A	XP_005250371.1:p.Gly332Asp
XM_006715967.1:c.1226G>A	XP_006716030.1:p.Gly409Asp
XM_006715968.1:c.1196G>A	XP_006716031.1:p.Gly399Asp
XM_006715969.1:c.1118G>A	XP_006716032.1:p.Gly373Asp
XM_006715970.2:c.1019G>A	XP_006716033.1:p.Gly340Asp
XM_006715971.1:c.995G>A	XP_006716034.1:p.Gly332Asp
XM_011516156.1:c.608G>A	XP_011514458.1:p.Gly203Asp
XM_011516157.1:c.608G>A	XP_011514459.1:p.Gly203Asp
XM_017012172.1:c.995G>A	XP_016867661.1:p.Gly332Asp
XM_017012173.1:c.1196G>A	XP_016867662.1:p.Gly399Asp
XM_024446755.1:c.1196G>A	XP_024302523.1:p.Gly399Asp
XM_024446756.1:c.1118G>A	XP_024302524.1:p.Gly373Asp
XM_024446757.1:c.1019G>A	XP_024302525.1:p.Gly340Asp
XM_024446758.1:c.995G>A	XP_024302526.1:p.Gly332Asp