Canonical Allele Identifier: CA369169469

Gene: IMPDH1

Linked Data

• MyVariant Identifiers: chr7:g.128038619G>A (hg19) ; chr7:g.128398565G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128398565G>A , CM000669.2:g.128398565G>A	GRCh38
NC_000007.13:g.128038619G>A , CM000669.1:g.128038619G>A	GRCh37
NC_000007.12:g.127825855G>A	NCBI36
NG_009194.1:g.16418C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348127.11:c.815C>T	ENSP00000265385.8:p.Ala272Val
ENST00000484496.6:n.798C>T
ENST00000338791.11:c.923C>T MANE Select	ENSP00000345096.6:p.Ala308Val
ENST00000648462.1:c.555C>T
ENST00000338791.10:c.923C>T	ENSP00000345096.6:p.Ala308Val
ENST00000348127.10:c.815C>T	ENSP00000265385.8:p.Ala272Val
ENST00000354269.9:c.893C>T	ENSP00000346219.5:p.Ala298Val
ENST00000419067.6:c.824C>T	ENSP00000399400.2:p.Ala275Val
ENST00000468842.1:n.512C>T
ENST00000469328.5:c.688C>T
ENST00000470772.5:c.665C>T	ENSP00000417296.1:p.Ala222Val
ENST00000480861.5:c.653C>T	ENSP00000420185.1:p.Ala218Val
ENST00000484496.5:c.798C>T	ENSP00000418742.1:n.798C>T
ENST00000496200.5:c.593C>T	ENSP00000420803.1:p.Ala198Val
ENST00000497868.5:c.716C>T	ENSP00000419609.1:p.Ala239Val
ENST00000626419.2:c.665C>T	ENSP00000486056.1:p.Ala222Val
NM_000883.3:c.923C>T	NP_000874.2:p.Ala308Val
NM_001102605.1:c.893C>T	NP_001096075.1:p.Ala298Val
NM_001142573.1:c.668C>T	NP_001136045.1:p.Ala223Val
NM_001142574.1:c.653C>T	NP_001136046.1:p.Ala218Val
NM_001142575.1:c.593C>T	NP_001136047.1:p.Ala198Val
NM_001142576.1:c.824C>T	NP_001136048.1:p.Ala275Val
NM_001304521.1:c.716C>T	NP_001291450.1:p.Ala239Val
NM_183243.2:c.815C>T	NP_899066.1:p.Ala272Val
XM_005250314.1:c.692C>T	XP_005250371.1:p.Ala231Val
XM_006715967.1:c.923C>T	XP_006716030.1:p.Ala308Val
XM_006715968.1:c.893C>T	XP_006716031.1:p.Ala298Val
XM_006715969.1:c.815C>T	XP_006716032.1:p.Ala272Val
XM_006715970.2:c.716C>T	XP_006716033.1:p.Ala239Val
XM_006715971.1:c.692C>T	XP_006716034.1:p.Ala231Val
XM_011516156.1:c.305C>T	XP_011514458.1:p.Ala102Val
XM_011516157.1:c.305C>T	XP_011514459.1:p.Ala102Val
XM_017012172.1:c.692C>T	XP_016867661.1:p.Ala231Val
XM_017012173.1:c.893C>T	XP_016867662.1:p.Ala298Val
XM_024446755.1:c.893C>T	XP_024302523.1:p.Ala298Val
XM_024446756.1:c.815C>T	XP_024302524.1:p.Ala272Val
XM_024446757.1:c.716C>T	XP_024302525.1:p.Ala239Val
XM_024446758.1:c.692C>T	XP_024302526.1:p.Ala231Val
NM_000883.4:c.923C>T MANE Select	NP_000874.2:p.Ala308Val
NM_001102605.2:c.893C>T	NP_001096075.1:p.Ala298Val
NM_001142573.2:c.668C>T	NP_001136045.1:p.Ala223Val
NM_001142574.2:c.653C>T	NP_001136046.1:p.Ala218Val
NM_001142575.2:c.593C>T	NP_001136047.1:p.Ala198Val
NM_001142576.2:c.824C>T	NP_001136048.1:p.Ala275Val
NM_001304521.2:c.716C>T	NP_001291450.1:p.Ala239Val
NM_183243.3:c.815C>T	NP_899066.1:p.Ala272Val