Canonical Allele Identifier: CA2683363011

Gene: HIP1

Linked Data

• gnomAD v4: 7-75581925-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75581925A>G , CM000669.2:g.75581925A>G	GRCh38
NC_000007.13:g.75211241A>G , CM000669.1:g.75211241A>G	GRCh37
NC_000007.12:g.75049177A>G	NCBI36
NG_023251.2:g.162037T>C
NG_023251.3:g.162037T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336926.11:c.542+150T>C MANE Select	ENSP00000336747.6:n.542+150T>C
ENST00000336926.10:c.542+150T>C	ENSP00000336747.6:n.542+150T>C
ENST00000434438.6:c.542+150T>C	ENSP00000410300.2:n.542+150T>C
ENST00000616821.4:c.455+150T>C	ENSP00000484528.1:n.455+150T>C
NM_001243198.2:c.542+150T>C	NP_001230127.1:n.542+150T>C
NM_005338.6:c.542+150T>C	NP_005329.3:n.542+150T>C
XM_005250304.2:c.455+150T>C	XP_005250361.1:n.455+150T>C
XM_005250305.2:c.440+150T>C	XP_005250362.1:n.440+150T>C
XM_011516116.1:c.542+150T>C	XP_011514418.1:n.542+150T>C
XM_011516116.2:c.542+150T>C	XP_011514418.1:n.542+150T>C
XM_017012099.1:c.500+150T>C	XP_016867588.1:n.500+150T>C
NM_005338.7:c.542+150T>C MANE Select	NP_005329.3:n.542+150T>C
NM_001243198.3:c.542+150T>C	NP_001230127.1:n.542+150T>C
NM_001382444.1:c.440+150T>C	NP_001369373.1:n.440+150T>C
NM_001382445.1:c.455+150T>C	NP_001369374.1:n.455+150T>C