Canonical Allele Identifier: CA1717985542

Gene: HIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75582024G= , CM000669.2:g.75582024G=	GRCh38
NC_000007.13:g.75211340G= , CM000669.1:g.75211340G=	GRCh37
NC_000007.12:g.75049276G=	NCBI36
NG_023251.2:g.161938C=
NG_023251.3:g.161938C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336926.11:c.542+51C= MANE Select	ENSP00000336747.6:n.542+51C=
ENST00000336926.10:c.542+51C=	ENSP00000336747.6:n.542+51C=
ENST00000434438.6:c.542+51C=	ENSP00000410300.2:n.542+51C=
ENST00000616821.4:c.455+51C=	ENSP00000484528.1:n.455+51C=
NM_001243198.2:c.542+51C=	NP_001230127.1:n.542+51C=
NM_005338.6:c.542+51C=	NP_005329.3:n.542+51C=
XM_005250304.2:c.455+51C=	XP_005250361.1:n.455+51C=
XM_005250305.2:c.440+51C=	XP_005250362.1:n.440+51C=
XM_011516116.1:c.542+51C=	XP_011514418.1:n.542+51C=
XM_011516116.2:c.542+51C=	XP_011514418.1:n.542+51C=
XM_017012099.1:c.500+51C=	XP_016867588.1:n.500+51C=
NM_005338.7:c.542+51C= MANE Select	NP_005329.3:n.542+51C=
NM_001243198.3:c.542+51C=	NP_001230127.1:n.542+51C=
NM_001382444.1:c.440+51C=	NP_001369373.1:n.440+51C=
NM_001382445.1:c.455+51C=	NP_001369374.1:n.455+51C=