Canonical Allele Identifier: CA369169517

Gene: IMPDH1

Linked Data

• MyVariant Identifiers: chr7:g.128038625A>C (hg19) ; chr7:g.128398571A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128398571A>C , CM000669.2:g.128398571A>C	GRCh38
NC_000007.13:g.128038625A>C , CM000669.1:g.128038625A>C	GRCh37
NC_000007.12:g.127825861A>C	NCBI36
NG_009194.1:g.16412T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.809T>G	ENSP00000265385.8:p.Ile270Ser
ENST00000484496.6:n.792T>G
ENST00000338791.11:c.917T>G MANE Select	ENSP00000345096.6:p.Ile306Ser
ENST00000648462.1:c.549T>G
ENST00000338791.10:c.917T>G	ENSP00000345096.6:p.Ile306Ser
ENST00000348127.10:c.809T>G	ENSP00000265385.8:p.Ile270Ser
ENST00000354269.9:c.887T>G	ENSP00000346219.5:p.Ile296Ser
ENST00000419067.6:c.818T>G	ENSP00000399400.2:p.Ile273Ser
ENST00000468842.1:n.506T>G
ENST00000469328.5:c.682T>G
ENST00000470772.5:c.659T>G	ENSP00000417296.1:p.Ile220Ser
ENST00000480861.5:c.647T>G	ENSP00000420185.1:p.Ile216Ser
ENST00000484496.5:c.792T>G	ENSP00000418742.1:n.792T>G
ENST00000496200.5:c.587T>G	ENSP00000420803.1:p.Ile196Ser
ENST00000497868.5:c.710T>G	ENSP00000419609.1:p.Ile237Ser
ENST00000626419.2:c.659T>G	ENSP00000486056.1:p.Ile220Ser
NM_000883.3:c.917T>G	NP_000874.2:p.Ile306Ser
NM_001102605.1:c.887T>G	NP_001096075.1:p.Ile296Ser
NM_001142573.1:c.662T>G	NP_001136045.1:p.Ile221Ser
NM_001142574.1:c.647T>G	NP_001136046.1:p.Ile216Ser
NM_001142575.1:c.587T>G	NP_001136047.1:p.Ile196Ser
NM_001142576.1:c.818T>G	NP_001136048.1:p.Ile273Ser
NM_001304521.1:c.710T>G	NP_001291450.1:p.Ile237Ser
NM_183243.2:c.809T>G	NP_899066.1:p.Ile270Ser
XM_005250314.1:c.686T>G	XP_005250371.1:p.Ile229Ser
XM_006715967.1:c.917T>G	XP_006716030.1:p.Ile306Ser
XM_006715968.1:c.887T>G	XP_006716031.1:p.Ile296Ser
XM_006715969.1:c.809T>G	XP_006716032.1:p.Ile270Ser
XM_006715970.2:c.710T>G	XP_006716033.1:p.Ile237Ser
XM_006715971.1:c.686T>G	XP_006716034.1:p.Ile229Ser
XM_011516156.1:c.299T>G	XP_011514458.1:p.Ile100Ser
XM_011516157.1:c.299T>G	XP_011514459.1:p.Ile100Ser
XM_017012172.1:c.686T>G	XP_016867661.1:p.Ile229Ser
XM_017012173.1:c.887T>G	XP_016867662.1:p.Ile296Ser
XM_024446755.1:c.887T>G	XP_024302523.1:p.Ile296Ser
XM_024446756.1:c.809T>G	XP_024302524.1:p.Ile270Ser
XM_024446757.1:c.710T>G	XP_024302525.1:p.Ile237Ser
XM_024446758.1:c.686T>G	XP_024302526.1:p.Ile229Ser
NM_000883.4:c.917T>G MANE Select	NP_000874.2:p.Ile306Ser
NM_001102605.2:c.887T>G	NP_001096075.1:p.Ile296Ser
NM_001142573.2:c.662T>G	NP_001136045.1:p.Ile221Ser
NM_001142574.2:c.647T>G	NP_001136046.1:p.Ile216Ser
NM_001142575.2:c.587T>G	NP_001136047.1:p.Ile196Ser
NM_001142576.2:c.818T>G	NP_001136048.1:p.Ile273Ser
NM_001304521.2:c.710T>G	NP_001291450.1:p.Ile237Ser
NM_183243.3:c.809T>G	NP_899066.1:p.Ile270Ser