Canonical Allele Identifier: CA2578914549
Gene: HIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75582116_75582117insGAC , CM000669.2:g.75582116_75582117insGAC GRCh38
NC_000007.13:g.75211432_75211433insGAC , CM000669.1:g.75211432_75211433insGAC GRCh37
NC_000007.12:g.75049368_75049369insGAC NCBI36
NG_023251.2:g.161845_161846insGTC
NG_023251.3:g.161845_161846insGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000336926.11:c.500_501insGTC MANE Select ENSP00000336747.6:p.Asp167delinsGluSer
ENST00000336926.10:c.500_501insGTC ENSP00000336747.6:p.Asp167delinsGluSer
ENST00000420909.1:c.413_414insGTC ENSP00000414280.1:p.Asp138delinsGluSer
ENST00000434438.6:c.500_501insGTC ENSP00000410300.2:p.Asp167delinsGluSer
ENST00000616821.4:c.413_414insGTC ENSP00000484528.1:p.Asp138delinsGluSer
NM_001243198.2:c.500_501insGTC NP_001230127.1:p.Asp167delinsGluSer
NM_005338.6:c.500_501insGTC NP_005329.3:p.Asp167delinsGluSer
XM_005250304.2:c.413_414insGTC XP_005250361.1:p.Asp138delinsGluSer
XM_005250305.2:c.398_399insGTC XP_005250362.1:p.Asp133delinsGluSer
XM_011516116.1:c.500_501insGTC XP_011514418.1:p.Asp167delinsGluSer
XM_011516116.2:c.500_501insGTC XP_011514418.1:p.Asp167delinsGluSer
XM_017012099.1:c.458_459insGTC XP_016867588.1:p.Asp153delinsGluSer
NM_005338.7:c.500_501insGTC MANE Select NP_005329.3:p.Asp167delinsGluSer
NM_001243198.3:c.500_501insGTC NP_001230127.1:p.Asp167delinsGluSer
NM_001382444.1:c.398_399insGTC NP_001369373.1:p.Asp133delinsGluSer
NM_001382445.1:c.413_414insGTC NP_001369374.1:p.Asp138delinsGluSer