Canonical Allele Identifier: CA457844176

Gene: IMPDH1

Linked Data

• MyVariant Identifiers: chr7:g.128034539A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128394485A>G , CM000669.2:g.128394485A>G	GRCh38
NC_000007.13:g.128034539A>G , CM000669.1:g.128034539A>G	GRCh37
NC_000007.12:g.127821775A>G	NCBI36
NG_009194.1:g.20498T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348127.11:c.1557T>C	ENSP00000265385.8:p.Asp519=
ENST00000484496.6:n.1540T>C
ENST00000338791.11:c.1665T>C MANE Select	ENSP00000345096.6:p.Asp555=
ENST00000648462.1:c.1297T>C
ENST00000338791.10:c.1665T>C	ENSP00000345096.6:p.Asp555=
ENST00000348127.10:c.1557T>C	ENSP00000265385.8:p.Asp519=
ENST00000354269.9:c.1635T>C	ENSP00000346219.5:p.Asp545=
ENST00000419067.6:c.1566T>C	ENSP00000399400.2:p.Asp522=
ENST00000460045.1:n.555T>C
ENST00000469328.5:c.1430T>C
ENST00000470772.5:c.1407T>C	ENSP00000417296.1:p.Asp469=
ENST00000480861.5:c.1395T>C	ENSP00000420185.1:p.Asp465=
ENST00000484496.5:c.1540T>C	ENSP00000418742.1:n.1540T>C
ENST00000496200.5:c.1335T>C	ENSP00000420803.1:p.Asp445=
ENST00000626419.2:c.1407T>C	ENSP00000486056.1:p.Asp469=
NM_000883.3:c.1665T>C	NP_000874.2:p.Asp555=
NM_001102605.1:c.1635T>C	NP_001096075.1:p.Asp545=
NM_001142573.1:c.1410T>C	NP_001136045.1:p.Asp470=
NM_001142574.1:c.1395T>C	NP_001136046.1:p.Asp465=
NM_001142575.1:c.1335T>C	NP_001136047.1:p.Asp445=
NM_001142576.1:c.1566T>C	NP_001136048.1:p.Asp522=
NM_001304521.1:c.1458T>C	NP_001291450.1:p.Asp486=
NM_183243.2:c.1557T>C	NP_899066.1:p.Asp519=
XM_005250314.1:c.1434T>C	XP_005250371.1:p.Asp478=
XM_006715967.1:c.1665T>C	XP_006716030.1:p.Asp555=
XM_006715968.1:c.1635T>C	XP_006716031.1:p.Asp545=
XM_006715969.1:c.1557T>C	XP_006716032.1:p.Asp519=
XM_006715970.2:c.1458T>C	XP_006716033.1:p.Asp486=
XM_006715971.1:c.1434T>C	XP_006716034.1:p.Asp478=
XM_011516156.1:c.1047T>C	XP_011514458.1:p.Asp349=
XM_011516157.1:c.1047T>C	XP_011514459.1:p.Asp349=
XM_017012172.1:c.1434T>C	XP_016867661.1:p.Asp478=
XM_024446755.1:c.1635T>C	XP_024302523.1:p.Asp545=
XM_024446756.1:c.1557T>C	XP_024302524.1:p.Asp519=
XM_024446757.1:c.1458T>C	XP_024302525.1:p.Asp486=
XM_024446758.1:c.1434T>C	XP_024302526.1:p.Asp478=
NM_000883.4:c.1665T>C MANE Select	NP_000874.2:p.Asp555=
NM_001102605.2:c.1635T>C	NP_001096075.1:p.Asp545=
NM_001142573.2:c.1410T>C	NP_001136045.1:p.Asp470=
NM_001142574.2:c.1395T>C	NP_001136046.1:p.Asp465=
NM_001142575.2:c.1335T>C	NP_001136047.1:p.Asp445=
NM_001142576.2:c.1566T>C	NP_001136048.1:p.Asp522=
NM_001304521.2:c.1458T>C	NP_001291450.1:p.Asp486=
NM_183243.3:c.1557T>C	NP_899066.1:p.Asp519=