Canonical Allele Identifier: CA2158501524
Community Standard Title: NM_001127258.3(HHIPL1):c.1649-617T=
Gene: HHIPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.99667605T= , CM000676.2:g.99667605T= GRCh38
NC_000014.8:g.100133942T= , CM000676.1:g.100133942T= GRCh37
NC_000014.7:g.99203695T= NCBI36
NG_051108.1:g.68130T=

Transcript Alleles

HGVS Amino-acid Change
NM_001127258.3:c.1649-617T= MANE Select NP_001120730.1:n.1649-617T=
ENST00000330710.10:c.1649-617T= MANE Select ENSP00000330601.5:n.1649-617T=
NM_001127258.1:c.1649-617T= NP_001120730.1:n.1649-617T=
NM_001127258.2:c.1649-617T= NP_001120730.1:n.1649-617T=
NM_001329411.1:c.1454-617T= NP_001316340.1:n.1454-617T=
NM_001329411.2:c.1454-617T= NP_001316340.1:n.1454-617T=
NM_032425.4:c.1649-617T= NP_115801.3:n.1649-617T=
NM_032425.5:c.1649-617T= NP_115801.3:n.1649-617T=
ENST00000330710.9:c.1649-617T= ENSP00000330601.5:n.1649-617T=
ENST00000357223.2:c.1649-617T= ENSP00000349757.2:n.1649-617T=
XM_006720277.2:c.1424-617T= XP_006720340.1:n.1424-617T=
XM_006720277.3:c.1424-617T= XP_006720340.1:n.1424-617T=
XM_011537236.1:c.1454-617T= XP_011535538.1:n.1454-617T=
XM_011537236.2:c.1454-617T= XP_011535538.1:n.1454-617T=
XM_011537237.1:c.1649-617T= XP_011535539.1:n.1649-617T=
XM_011537237.2:c.1649-617T= XP_011535539.1:n.1649-617T=
XM_017021707.2:c.1298-617T= XP_016877196.1:n.1298-617T=