Canonical Allele Identifier: CA369169830

Gene: IMPDH1

Linked Data

• MyVariant Identifiers: chr7:g.128038652A>T (hg19) ; chr7:g.128398598A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128398598A>T , CM000669.2:g.128398598A>T	GRCh38
NC_000007.13:g.128038652A>T , CM000669.1:g.128038652A>T	GRCh37
NC_000007.12:g.127825888A>T	NCBI36
NG_009194.1:g.16385T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.782T>A	ENSP00000265385.8:p.Val261Asp
ENST00000484496.6:n.765T>A
ENST00000338791.11:c.890T>A MANE Select	ENSP00000345096.6:p.Val297Asp
ENST00000648462.1:c.522T>A
ENST00000338791.10:c.890T>A	ENSP00000345096.6:p.Val297Asp
ENST00000348127.10:c.782T>A	ENSP00000265385.8:p.Val261Asp
ENST00000354269.9:c.860T>A	ENSP00000346219.5:p.Val287Asp
ENST00000419067.6:c.791T>A	ENSP00000399400.2:p.Val264Asp
ENST00000468842.1:n.479T>A
ENST00000469328.5:c.655T>A
ENST00000470772.5:c.632T>A	ENSP00000417296.1:p.Val211Asp
ENST00000480861.5:c.620T>A	ENSP00000420185.1:p.Val207Asp
ENST00000484496.5:c.765T>A	ENSP00000418742.1:n.765T>A
ENST00000496200.5:c.560T>A	ENSP00000420803.1:p.Val187Asp
ENST00000497868.5:c.683T>A	ENSP00000419609.1:p.Val228Asp
ENST00000626419.2:c.632T>A	ENSP00000486056.1:p.Val211Asp
NM_000883.3:c.890T>A	NP_000874.2:p.Val297Asp
NM_001102605.1:c.860T>A	NP_001096075.1:p.Val287Asp
NM_001142573.1:c.635T>A	NP_001136045.1:p.Val212Asp
NM_001142574.1:c.620T>A	NP_001136046.1:p.Val207Asp
NM_001142575.1:c.560T>A	NP_001136047.1:p.Val187Asp
NM_001142576.1:c.791T>A	NP_001136048.1:p.Val264Asp
NM_001304521.1:c.683T>A	NP_001291450.1:p.Val228Asp
NM_183243.2:c.782T>A	NP_899066.1:p.Val261Asp
XM_005250314.1:c.659T>A	XP_005250371.1:p.Val220Asp
XM_006715967.1:c.890T>A	XP_006716030.1:p.Val297Asp
XM_006715968.1:c.860T>A	XP_006716031.1:p.Val287Asp
XM_006715969.1:c.782T>A	XP_006716032.1:p.Val261Asp
XM_006715970.2:c.683T>A	XP_006716033.1:p.Val228Asp
XM_006715971.1:c.659T>A	XP_006716034.1:p.Val220Asp
XM_011516156.1:c.272T>A	XP_011514458.1:p.Val91Asp
XM_011516157.1:c.272T>A	XP_011514459.1:p.Val91Asp
XM_017012172.1:c.659T>A	XP_016867661.1:p.Val220Asp
XM_017012173.1:c.860T>A	XP_016867662.1:p.Val287Asp
XM_024446755.1:c.860T>A	XP_024302523.1:p.Val287Asp
XM_024446756.1:c.782T>A	XP_024302524.1:p.Val261Asp
XM_024446757.1:c.683T>A	XP_024302525.1:p.Val228Asp
XM_024446758.1:c.659T>A	XP_024302526.1:p.Val220Asp
NM_000883.4:c.890T>A MANE Select	NP_000874.2:p.Val297Asp
NM_001102605.2:c.860T>A	NP_001096075.1:p.Val287Asp
NM_001142573.2:c.635T>A	NP_001136045.1:p.Val212Asp
NM_001142574.2:c.620T>A	NP_001136046.1:p.Val207Asp
NM_001142575.2:c.560T>A	NP_001136047.1:p.Val187Asp
NM_001142576.2:c.791T>A	NP_001136048.1:p.Val264Asp
NM_001304521.2:c.683T>A	NP_001291450.1:p.Val228Asp
NM_183243.3:c.782T>A	NP_899066.1:p.Val261Asp