Canonical Allele Identifier: CA4302611

Gene: HIP1

Linked Data

• dbSNP Id: rs782533052
• ExAC: 7:75211461 T / G
• gnomAD v2: 7-75211461-T-G
• gnomAD v3: 7-75582145-T-G
• gnomAD v4: 7-75582145-T-G
• MyVariant Identifiers: chr7:g.75211461T>G (hg19) ; chr7:g.75582145T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75582145T>G , CM000669.2:g.75582145T>G	GRCh38
NC_000007.13:g.75211461T>G , CM000669.1:g.75211461T>G	GRCh37
NC_000007.12:g.75049397T>G	NCBI36
NG_023251.2:g.161817A>C
NG_023251.3:g.161817A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336926.11:c.472A>C MANE Select	ENSP00000336747.6:p.Arg158=
ENST00000336926.10:c.472A>C	ENSP00000336747.6:p.Arg158=
ENST00000420909.1:c.385A>C	ENSP00000414280.1:p.Arg129=
ENST00000434438.6:c.472A>C	ENSP00000410300.2:p.Arg158=
ENST00000616821.4:c.385A>C	ENSP00000484528.1:p.Arg129=
NM_001243198.2:c.472A>C	NP_001230127.1:p.Arg158=
NM_005338.6:c.472A>C	NP_005329.3:p.Arg158=
XM_005250304.2:c.385A>C	XP_005250361.1:p.Arg129=
XM_005250305.2:c.370A>C	XP_005250362.1:p.Arg124=
XM_011516116.1:c.472A>C	XP_011514418.1:p.Arg158=
XM_011516116.2:c.472A>C	XP_011514418.1:p.Arg158=
XM_017012099.1:c.430A>C	XP_016867588.1:p.Arg144=
NM_005338.7:c.472A>C MANE Select	NP_005329.3:p.Arg158=
NM_001243198.3:c.472A>C	NP_001230127.1:p.Arg158=
NM_001382444.1:c.370A>C	NP_001369373.1:p.Arg124=
NM_001382445.1:c.385A>C	NP_001369374.1:p.Arg129=