Canonical Allele Identifier: CA369168400

Gene: IMPDH1

Linked Data

• gnomAD v4: 7-128398467-C-A
• MyVariant Identifiers: chr7:g.128038521C>A (hg19) ; chr7:g.128398467C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128398467C>A , CM000669.2:g.128398467C>A	GRCh38
NC_000007.13:g.128038521C>A , CM000669.1:g.128038521C>A	GRCh37
NC_000007.12:g.127825757C>A	NCBI36
NG_009194.1:g.16516G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348127.11:c.913G>T	ENSP00000265385.8:p.Asp305Tyr
ENST00000484496.6:n.896G>T
ENST00000338791.11:c.1021G>T MANE Select	ENSP00000345096.6:p.Asp341Tyr
ENST00000648462.1:c.653G>T
ENST00000338791.10:c.1021G>T	ENSP00000345096.6:p.Asp341Tyr
ENST00000348127.10:c.913G>T	ENSP00000265385.8:p.Asp305Tyr
ENST00000354269.9:c.991G>T	ENSP00000346219.5:p.Asp331Tyr
ENST00000419067.6:c.922G>T	ENSP00000399400.2:p.Asp308Tyr
ENST00000469328.5:c.786G>T
ENST00000470772.5:c.763G>T	ENSP00000417296.1:p.Asp255Tyr
ENST00000480861.5:c.751G>T	ENSP00000420185.1:p.Asp251Tyr
ENST00000484496.5:c.896G>T	ENSP00000418742.1:n.896G>T
ENST00000496200.5:c.691G>T	ENSP00000420803.1:p.Asp231Tyr
ENST00000497868.5:c.814G>T	ENSP00000419609.1:p.Asp272Tyr
ENST00000626419.2:c.763G>T	ENSP00000486056.1:p.Asp255Tyr
NM_000883.3:c.1021G>T	NP_000874.2:p.Asp341Tyr
NM_001102605.1:c.991G>T	NP_001096075.1:p.Asp331Tyr
NM_001142573.1:c.766G>T	NP_001136045.1:p.Asp256Tyr
NM_001142574.1:c.751G>T	NP_001136046.1:p.Asp251Tyr
NM_001142575.1:c.691G>T	NP_001136047.1:p.Asp231Tyr
NM_001142576.1:c.922G>T	NP_001136048.1:p.Asp308Tyr
NM_001304521.1:c.814G>T	NP_001291450.1:p.Asp272Tyr
NM_183243.2:c.913G>T	NP_899066.1:p.Asp305Tyr
XM_005250314.1:c.790G>T	XP_005250371.1:p.Asp264Tyr
XM_006715967.1:c.1021G>T	XP_006716030.1:p.Asp341Tyr
XM_006715968.1:c.991G>T	XP_006716031.1:p.Asp331Tyr
XM_006715969.1:c.913G>T	XP_006716032.1:p.Asp305Tyr
XM_006715970.2:c.814G>T	XP_006716033.1:p.Asp272Tyr
XM_006715971.1:c.790G>T	XP_006716034.1:p.Asp264Tyr
XM_011516156.1:c.403G>T	XP_011514458.1:p.Asp135Tyr
XM_011516157.1:c.403G>T	XP_011514459.1:p.Asp135Tyr
XM_017012172.1:c.790G>T	XP_016867661.1:p.Asp264Tyr
XM_017012173.1:c.991G>T	XP_016867662.1:p.Asp331Tyr
XM_024446755.1:c.991G>T	XP_024302523.1:p.Asp331Tyr
XM_024446756.1:c.913G>T	XP_024302524.1:p.Asp305Tyr
XM_024446757.1:c.814G>T	XP_024302525.1:p.Asp272Tyr
XM_024446758.1:c.790G>T	XP_024302526.1:p.Asp264Tyr
NM_000883.4:c.1021G>T MANE Select	NP_000874.2:p.Asp341Tyr
NM_001102605.2:c.991G>T	NP_001096075.1:p.Asp331Tyr
NM_001142573.2:c.766G>T	NP_001136045.1:p.Asp256Tyr
NM_001142574.2:c.751G>T	NP_001136046.1:p.Asp251Tyr
NM_001142575.2:c.691G>T	NP_001136047.1:p.Asp231Tyr
NM_001142576.2:c.922G>T	NP_001136048.1:p.Asp308Tyr
NM_001304521.2:c.814G>T	NP_001291450.1:p.Asp272Tyr
NM_183243.3:c.913G>T	NP_899066.1:p.Asp305Tyr