Canonical Allele Identifier: CA457528361

Gene: IMPDH1

Linked Data

• dbSNP Id: rs1798092391
• gnomAD v3: 7-128398561-G-A
• gnomAD v4: 7-128398561-G-A
• MyVariant Identifiers: chr7:g.128038615G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128398561G>A , CM000669.2:g.128398561G>A	GRCh38
NC_000007.13:g.128038615G>A , CM000669.1:g.128038615G>A	GRCh37
NC_000007.12:g.127825851G>A	NCBI36
NG_009194.1:g.16422C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348127.11:c.819C>T	ENSP00000265385.8:p.Arg273=
ENST00000484496.6:n.802C>T
ENST00000338791.11:c.927C>T MANE Select	ENSP00000345096.6:p.Arg309=
ENST00000648462.1:c.559C>T
ENST00000338791.10:c.927C>T	ENSP00000345096.6:p.Arg309=
ENST00000348127.10:c.819C>T	ENSP00000265385.8:p.Arg273=
ENST00000354269.9:c.897C>T	ENSP00000346219.5:p.Arg299=
ENST00000419067.6:c.828C>T	ENSP00000399400.2:p.Arg276=
ENST00000468842.1:n.516C>T
ENST00000469328.5:c.692C>T
ENST00000470772.5:c.669C>T	ENSP00000417296.1:p.Arg223=
ENST00000480861.5:c.657C>T	ENSP00000420185.1:p.Arg219=
ENST00000484496.5:c.802C>T	ENSP00000418742.1:n.802C>T
ENST00000496200.5:c.597C>T	ENSP00000420803.1:p.Arg199=
ENST00000497868.5:c.720C>T	ENSP00000419609.1:p.Arg240=
ENST00000626419.2:c.669C>T	ENSP00000486056.1:p.Arg223=
NM_000883.3:c.927C>T	NP_000874.2:p.Arg309=
NM_001102605.1:c.897C>T	NP_001096075.1:p.Arg299=
NM_001142573.1:c.672C>T	NP_001136045.1:p.Arg224=
NM_001142574.1:c.657C>T	NP_001136046.1:p.Arg219=
NM_001142575.1:c.597C>T	NP_001136047.1:p.Arg199=
NM_001142576.1:c.828C>T	NP_001136048.1:p.Arg276=
NM_001304521.1:c.720C>T	NP_001291450.1:p.Arg240=
NM_183243.2:c.819C>T	NP_899066.1:p.Arg273=
XM_005250314.1:c.696C>T	XP_005250371.1:p.Arg232=
XM_006715967.1:c.927C>T	XP_006716030.1:p.Arg309=
XM_006715968.1:c.897C>T	XP_006716031.1:p.Arg299=
XM_006715969.1:c.819C>T	XP_006716032.1:p.Arg273=
XM_006715970.2:c.720C>T	XP_006716033.1:p.Arg240=
XM_006715971.1:c.696C>T	XP_006716034.1:p.Arg232=
XM_011516156.1:c.309C>T	XP_011514458.1:p.Arg103=
XM_011516157.1:c.309C>T	XP_011514459.1:p.Arg103=
XM_017012172.1:c.696C>T	XP_016867661.1:p.Arg232=
XM_017012173.1:c.897C>T	XP_016867662.1:p.Arg299=
XM_024446755.1:c.897C>T	XP_024302523.1:p.Arg299=
XM_024446756.1:c.819C>T	XP_024302524.1:p.Arg273=
XM_024446757.1:c.720C>T	XP_024302525.1:p.Arg240=
XM_024446758.1:c.696C>T	XP_024302526.1:p.Arg232=
NM_000883.4:c.927C>T MANE Select	NP_000874.2:p.Arg309=
NM_001102605.2:c.897C>T	NP_001096075.1:p.Arg299=
NM_001142573.2:c.672C>T	NP_001136045.1:p.Arg224=
NM_001142574.2:c.657C>T	NP_001136046.1:p.Arg219=
NM_001142575.2:c.597C>T	NP_001136047.1:p.Arg199=
NM_001142576.2:c.828C>T	NP_001136048.1:p.Arg276=
NM_001304521.2:c.720C>T	NP_001291450.1:p.Arg240=
NM_183243.3:c.819C>T	NP_899066.1:p.Arg273=