Canonical Allele Identifier: CA4027618

Gene: HIVEP2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.142753590A>T , CM000668.2:g.142753590A>T	GRCh38
NC_000006.11:g.143074727A>T , CM000668.1:g.143074727A>T	GRCh37
NC_000006.10:g.143116420A>T	NCBI36
NG_047004.1:g.196612T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703916.1:c.1671T>A	ENSP00000515550.1:p.Gly557=
ENST00000703917.1:c.1671T>A	ENSP00000515551.1:p.Gly557=
ENST00000703918.1:c.6858T>A	ENSP00000515552.1:p.Gly2286=
ENST00000012134.7:c.6858T>A	ENSP00000012134.2:p.Gly2286=
ENST00000367603.8:c.6858T>A MANE Select	ENSP00000356575.2:p.Gly2286=
ENST00000367604.6:c.6858T>A	ENSP00000356576.1:p.Gly2286=
ENST00000012134.6:c.6858T>A	ENSP00000012134.2:p.Gly2286=
ENST00000367603.6:c.6858T>A	ENSP00000356575.2:p.Gly2286=
ENST00000367604.5:c.6858T>A	ENSP00000356576.1:p.Gly2286=
NM_006734.3:c.6858T>A	NP_006725.3:p.Gly2286=
XM_017010805.1:c.6858T>A	XP_016866294.1:p.Gly2286=
XM_024446416.1:c.6858T>A	XP_024302184.1:p.Gly2286=
XM_024446417.1:c.6858T>A	XP_024302185.1:p.Gly2286=
XM_024446418.1:c.6858T>A	XP_024302186.1:p.Gly2286=
XM_024446419.1:c.6858T>A	XP_024302187.1:p.Gly2286=
NM_006734.4:c.6858T>A MANE Select	NP_006725.3:p.Gly2286=