Canonical Allele Identifier: CA2683363300

Gene: HIP1

Linked Data

• gnomAD v4: 7-75582026-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75582026A>T , CM000669.2:g.75582026A>T	GRCh38
NC_000007.13:g.75211342A>T , CM000669.1:g.75211342A>T	GRCh37
NC_000007.12:g.75049278A>T	NCBI36
NG_023251.2:g.161936T>A
NG_023251.3:g.161936T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336926.11:c.542+49T>A MANE Select	ENSP00000336747.6:n.542+49T>A
ENST00000336926.10:c.542+49T>A	ENSP00000336747.6:n.542+49T>A
ENST00000434438.6:c.542+49T>A	ENSP00000410300.2:n.542+49T>A
ENST00000616821.4:c.455+49T>A	ENSP00000484528.1:n.455+49T>A
NM_001243198.2:c.542+49T>A	NP_001230127.1:n.542+49T>A
NM_005338.6:c.542+49T>A	NP_005329.3:n.542+49T>A
XM_005250304.2:c.455+49T>A	XP_005250361.1:n.455+49T>A
XM_005250305.2:c.440+49T>A	XP_005250362.1:n.440+49T>A
XM_011516116.1:c.542+49T>A	XP_011514418.1:n.542+49T>A
XM_011516116.2:c.542+49T>A	XP_011514418.1:n.542+49T>A
XM_017012099.1:c.500+49T>A	XP_016867588.1:n.500+49T>A
NM_005338.7:c.542+49T>A MANE Select	NP_005329.3:n.542+49T>A
NM_001243198.3:c.542+49T>A	NP_001230127.1:n.542+49T>A
NM_001382444.1:c.440+49T>A	NP_001369373.1:n.440+49T>A
NM_001382445.1:c.455+49T>A	NP_001369374.1:n.455+49T>A