Canonical Allele Identifier: CA1717985627

Gene: HIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75582115G= , CM000669.2:g.75582115G=	GRCh38
NC_000007.13:g.75211431G= , CM000669.1:g.75211431G=	GRCh37
NC_000007.12:g.75049367G=	NCBI36
NG_023251.2:g.161847C=
NG_023251.3:g.161847C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336926.11:c.502C= MANE Select	ENSP00000336747.6:p.Arg168=
ENST00000336926.10:c.502C=	ENSP00000336747.6:p.Arg168=
ENST00000420909.1:c.415C=	ENSP00000414280.1:p.Arg139=
ENST00000434438.6:c.502C=	ENSP00000410300.2:p.Arg168=
ENST00000616821.4:c.415C=	ENSP00000484528.1:p.Arg139=
NM_001243198.2:c.502C=	NP_001230127.1:p.Arg168=
NM_005338.6:c.502C=	NP_005329.3:p.Arg168=
XM_005250304.2:c.415C=	XP_005250361.1:p.Arg139=
XM_005250305.2:c.400C=	XP_005250362.1:p.Arg134=
XM_011516116.1:c.502C=	XP_011514418.1:p.Arg168=
XM_011516116.2:c.502C=	XP_011514418.1:p.Arg168=
XM_017012099.1:c.460C=	XP_016867588.1:p.Arg154=
NM_005338.7:c.502C= MANE Select	NP_005329.3:p.Arg168=
NM_001243198.3:c.502C=	NP_001230127.1:p.Arg168=
NM_001382444.1:c.400C=	NP_001369373.1:p.Arg134=
NM_001382445.1:c.415C=	NP_001369374.1:p.Arg139=