Canonical Allele Identifier: CA1717985625

Gene: HIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75582114C= , CM000669.2:g.75582114C=	GRCh38
NC_000007.13:g.75211430C= , CM000669.1:g.75211430C=	GRCh37
NC_000007.12:g.75049366C=	NCBI36
NG_023251.2:g.161848G=
NG_023251.3:g.161848G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336926.11:c.503G= MANE Select	ENSP00000336747.6:p.Arg168=
ENST00000336926.10:c.503G=	ENSP00000336747.6:p.Arg168=
ENST00000420909.1:c.416G=	ENSP00000414280.1:p.Arg139=
ENST00000434438.6:c.503G=	ENSP00000410300.2:p.Arg168=
ENST00000616821.4:c.416G=	ENSP00000484528.1:p.Arg139=
NM_001243198.2:c.503G=	NP_001230127.1:p.Arg168=
NM_005338.6:c.503G=	NP_005329.3:p.Arg168=
XM_005250304.2:c.416G=	XP_005250361.1:p.Arg139=
XM_005250305.2:c.401G=	XP_005250362.1:p.Arg134=
XM_011516116.1:c.503G=	XP_011514418.1:p.Arg168=
XM_011516116.2:c.503G=	XP_011514418.1:p.Arg168=
XM_017012099.1:c.461G=	XP_016867588.1:p.Arg154=
NM_005338.7:c.503G= MANE Select	NP_005329.3:p.Arg168=
NM_001243198.3:c.503G=	NP_001230127.1:p.Arg168=
NM_001382444.1:c.401G=	NP_001369373.1:p.Arg134=
NM_001382445.1:c.416G=	NP_001369374.1:p.Arg139=