Canonical Allele Identifier: CA455709899

Gene: HIP1

Linked Data

• gnomAD v4: 7-75582095-T-C
• MyVariant Identifiers: chr7:g.75211411T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75582095T>C , CM000669.2:g.75582095T>C	GRCh38
NC_000007.13:g.75211411T>C , CM000669.1:g.75211411T>C	GRCh37
NC_000007.12:g.75049347T>C	NCBI36
NG_023251.2:g.161867A>G
NG_023251.3:g.161867A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336926.11:c.522A>G MANE Select	ENSP00000336747.6:p.Gly174=
ENST00000336926.10:c.522A>G	ENSP00000336747.6:p.Gly174=
ENST00000420909.1:c.435A>G	ENSP00000414280.1:p.Gly145=
ENST00000434438.6:c.522A>G	ENSP00000410300.2:p.Gly174=
ENST00000616821.4:c.435A>G	ENSP00000484528.1:p.Gly145=
NM_001243198.2:c.522A>G	NP_001230127.1:p.Gly174=
NM_005338.6:c.522A>G	NP_005329.3:p.Gly174=
XM_005250304.2:c.435A>G	XP_005250361.1:p.Gly145=
XM_005250305.2:c.420A>G	XP_005250362.1:p.Gly140=
XM_011516116.1:c.522A>G	XP_011514418.1:p.Gly174=
XM_011516116.2:c.522A>G	XP_011514418.1:p.Gly174=
XM_017012099.1:c.480A>G	XP_016867588.1:p.Gly160=
NM_005338.7:c.522A>G MANE Select	NP_005329.3:p.Gly174=
NM_001243198.3:c.522A>G	NP_001230127.1:p.Gly174=
NM_001382444.1:c.420A>G	NP_001369373.1:p.Gly140=
NM_001382445.1:c.435A>G	NP_001369374.1:p.Gly145=