Canonical Allele Identifier: CA457528597

Gene: IMPDH1

Linked Data

• MyVariant Identifiers: chr7:g.128041105G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128401051G>A , CM000669.2:g.128401051G>A	GRCh38
NC_000007.13:g.128041105G>A , CM000669.1:g.128041105G>A	GRCh37
NC_000007.12:g.127828341G>A	NCBI36
NG_009194.1:g.13932C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348127.11:c.360C>T	ENSP00000265385.8:p.Asp120=
ENST00000484496.6:n.324C>T
ENST00000338791.11:c.468C>T MANE Select	ENSP00000345096.6:p.Asp156=
ENST00000648462.1:c.115C>T
ENST00000338791.10:c.468C>T	ENSP00000345096.6:p.Asp156=
ENST00000348127.10:c.360C>T	ENSP00000265385.8:p.Asp120=
ENST00000354269.9:c.438C>T	ENSP00000346219.5:p.Asp146=
ENST00000419067.6:c.369C>T	ENSP00000399400.2:p.Asp123=
ENST00000469328.5:c.214C>T
ENST00000470772.5:c.213C>T	ENSP00000417296.1:p.Asp71=
ENST00000473463.1:c.*214C>T	ENSP00000420469.1:n.*214C>T
ENST00000480861.5:c.213C>T	ENSP00000420185.1:p.Asp71=
ENST00000484496.5:c.324C>T	ENSP00000418742.1:p.Asp108=
ENST00000489263.1:c.261C>T	ENSP00000418592.1:p.Asp87=
ENST00000491376.5:n.637C>T
ENST00000496200.5:c.213C>T	ENSP00000420803.1:p.Asp71=
ENST00000496487.5:n.288C>T
ENST00000497868.5:c.261C>T	ENSP00000419609.1:p.Asp87=
ENST00000626419.2:c.213C>T	ENSP00000486056.1:p.Asp71=
NM_000883.3:c.468C>T	NP_000874.2:p.Asp156=
NM_001102605.1:c.438C>T	NP_001096075.1:p.Asp146=
NM_001142573.1:c.213C>T	NP_001136045.1:p.Asp71=
NM_001142574.1:c.213C>T	NP_001136046.1:p.Asp71=
NM_001142575.1:c.213C>T	NP_001136047.1:p.Asp71=
NM_001142576.1:c.369C>T	NP_001136048.1:p.Asp123=
NM_001304521.1:c.261C>T	NP_001291450.1:p.Asp87=
NM_183243.2:c.360C>T	NP_899066.1:p.Asp120=
XM_005250314.1:c.237C>T	XP_005250371.1:p.Asp79=
XM_006715967.1:c.468C>T	XP_006716030.1:p.Asp156=
XM_006715968.1:c.438C>T	XP_006716031.1:p.Asp146=
XM_006715969.1:c.360C>T	XP_006716032.1:p.Asp120=
XM_006715970.2:c.261C>T	XP_006716033.1:p.Asp87=
XM_006715971.1:c.237C>T	XP_006716034.1:p.Asp79=
XM_017012172.1:c.237C>T	XP_016867661.1:p.Asp79=
XM_017012173.1:c.438C>T	XP_016867662.1:p.Asp146=
XM_024446755.1:c.438C>T	XP_024302523.1:p.Asp146=
XM_024446756.1:c.360C>T	XP_024302524.1:p.Asp120=
XM_024446757.1:c.261C>T	XP_024302525.1:p.Asp87=
XM_024446758.1:c.237C>T	XP_024302526.1:p.Asp79=
NM_000883.4:c.468C>T MANE Select	NP_000874.2:p.Asp156=
NM_001102605.2:c.438C>T	NP_001096075.1:p.Asp146=
NM_001142573.2:c.213C>T	NP_001136045.1:p.Asp71=
NM_001142574.2:c.213C>T	NP_001136046.1:p.Asp71=
NM_001142575.2:c.213C>T	NP_001136047.1:p.Asp71=
NM_001142576.2:c.369C>T	NP_001136048.1:p.Asp123=
NM_001304521.2:c.261C>T	NP_001291450.1:p.Asp87=
NM_183243.3:c.360C>T	NP_899066.1:p.Asp120=