Canonical Allele Identifier: CA710538107

Gene: HHIPL1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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