Canonical Allele Identifier: CA1717985623
Gene: HIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75582109G= , CM000669.2:g.75582109G= GRCh38
NC_000007.13:g.75211425G= , CM000669.1:g.75211425G= GRCh37
NC_000007.12:g.75049361G= NCBI36
NG_023251.2:g.161853C=
NG_023251.3:g.161853C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336926.11:c.508C= MANE Select ENSP00000336747.6:p.Leu170=
ENST00000336926.10:c.508C= ENSP00000336747.6:p.Leu170=
ENST00000420909.1:c.421C= ENSP00000414280.1:p.Leu141=
ENST00000434438.6:c.508C= ENSP00000410300.2:p.Leu170=
ENST00000616821.4:c.421C= ENSP00000484528.1:p.Leu141=
NM_001243198.2:c.508C= NP_001230127.1:p.Leu170=
NM_005338.6:c.508C= NP_005329.3:p.Leu170=
XM_005250304.2:c.421C= XP_005250361.1:p.Leu141=
XM_005250305.2:c.406C= XP_005250362.1:p.Leu136=
XM_011516116.1:c.508C= XP_011514418.1:p.Leu170=
XM_011516116.2:c.508C= XP_011514418.1:p.Leu170=
XM_017012099.1:c.466C= XP_016867588.1:p.Leu156=
NM_005338.7:c.508C= MANE Select NP_005329.3:p.Leu170=
NM_001243198.3:c.508C= NP_001230127.1:p.Leu170=
NM_001382444.1:c.406C= NP_001369373.1:p.Leu136=
NM_001382445.1:c.421C= NP_001369374.1:p.Leu141=