Canonical Allele Identifier: CA369162038

Gene: IMPDH1

Linked Data

• MyVariant Identifiers: chr7:g.128034540T>A (hg19) ; chr7:g.128394486T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128394486T>A , CM000669.2:g.128394486T>A	GRCh38
NC_000007.13:g.128034540T>A , CM000669.1:g.128034540T>A	GRCh37
NC_000007.12:g.127821776T>A	NCBI36
NG_009194.1:g.20497A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348127.11:c.1556A>T	ENSP00000265385.8:p.Asp519Val
ENST00000484496.6:n.1539A>T
ENST00000338791.11:c.1664A>T MANE Select	ENSP00000345096.6:p.Asp555Val
ENST00000648462.1:c.1296A>T
ENST00000338791.10:c.1664A>T	ENSP00000345096.6:p.Asp555Val
ENST00000348127.10:c.1556A>T	ENSP00000265385.8:p.Asp519Val
ENST00000354269.9:c.1634A>T	ENSP00000346219.5:p.Asp545Val
ENST00000419067.6:c.1565A>T	ENSP00000399400.2:p.Asp522Val
ENST00000460045.1:n.554A>T
ENST00000469328.5:c.1429A>T
ENST00000470772.5:c.1406A>T	ENSP00000417296.1:p.Asp469Val
ENST00000480861.5:c.1394A>T	ENSP00000420185.1:p.Asp465Val
ENST00000484496.5:c.1539A>T	ENSP00000418742.1:n.1539A>T
ENST00000496200.5:c.1334A>T	ENSP00000420803.1:p.Asp445Val
ENST00000626419.2:c.1406A>T	ENSP00000486056.1:p.Asp469Val
NM_000883.3:c.1664A>T	NP_000874.2:p.Asp555Val
NM_001102605.1:c.1634A>T	NP_001096075.1:p.Asp545Val
NM_001142573.1:c.1409A>T	NP_001136045.1:p.Asp470Val
NM_001142574.1:c.1394A>T	NP_001136046.1:p.Asp465Val
NM_001142575.1:c.1334A>T	NP_001136047.1:p.Asp445Val
NM_001142576.1:c.1565A>T	NP_001136048.1:p.Asp522Val
NM_001304521.1:c.1457A>T	NP_001291450.1:p.Asp486Val
NM_183243.2:c.1556A>T	NP_899066.1:p.Asp519Val
XM_005250314.1:c.1433A>T	XP_005250371.1:p.Asp478Val
XM_006715967.1:c.1664A>T	XP_006716030.1:p.Asp555Val
XM_006715968.1:c.1634A>T	XP_006716031.1:p.Asp545Val
XM_006715969.1:c.1556A>T	XP_006716032.1:p.Asp519Val
XM_006715970.2:c.1457A>T	XP_006716033.1:p.Asp486Val
XM_006715971.1:c.1433A>T	XP_006716034.1:p.Asp478Val
XM_011516156.1:c.1046A>T	XP_011514458.1:p.Asp349Val
XM_011516157.1:c.1046A>T	XP_011514459.1:p.Asp349Val
XM_017012172.1:c.1433A>T	XP_016867661.1:p.Asp478Val
XM_024446755.1:c.1634A>T	XP_024302523.1:p.Asp545Val
XM_024446756.1:c.1556A>T	XP_024302524.1:p.Asp519Val
XM_024446757.1:c.1457A>T	XP_024302525.1:p.Asp486Val
XM_024446758.1:c.1433A>T	XP_024302526.1:p.Asp478Val
NM_000883.4:c.1664A>T MANE Select	NP_000874.2:p.Asp555Val
NM_001102605.2:c.1634A>T	NP_001096075.1:p.Asp545Val
NM_001142573.2:c.1409A>T	NP_001136045.1:p.Asp470Val
NM_001142574.2:c.1394A>T	NP_001136046.1:p.Asp465Val
NM_001142575.2:c.1334A>T	NP_001136047.1:p.Asp445Val
NM_001142576.2:c.1565A>T	NP_001136048.1:p.Asp522Val
NM_001304521.2:c.1457A>T	NP_001291450.1:p.Asp486Val
NM_183243.3:c.1556A>T	NP_899066.1:p.Asp519Val