Canonical Allele Identifier: CA367726937

Gene: HIP1

Linked Data

• MyVariant Identifiers: chr7:g.75211401C>G (hg19) ; chr7:g.75582085C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75582085C>G , CM000669.2:g.75582085C>G	GRCh38
NC_000007.13:g.75211401C>G , CM000669.1:g.75211401C>G	GRCh37
NC_000007.12:g.75049337C>G	NCBI36
NG_023251.2:g.161877G>C
NG_023251.3:g.161877G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336926.11:c.532G>C MANE Select	ENSP00000336747.6:p.Val178Leu
ENST00000336926.10:c.532G>C	ENSP00000336747.6:p.Val178Leu
ENST00000434438.6:c.532G>C	ENSP00000410300.2:p.Val178Leu
ENST00000616821.4:c.445G>C	ENSP00000484528.1:p.Val149Leu
NM_001243198.2:c.532G>C	NP_001230127.1:p.Val178Leu
NM_005338.6:c.532G>C	NP_005329.3:p.Val178Leu
XM_005250304.2:c.445G>C	XP_005250361.1:p.Val149Leu
XM_005250305.2:c.430G>C	XP_005250362.1:p.Val144Leu
XM_011516116.1:c.532G>C	XP_011514418.1:p.Val178Leu
XM_011516116.2:c.532G>C	XP_011514418.1:p.Val178Leu
XM_017012099.1:c.490G>C	XP_016867588.1:p.Val164Leu
NM_005338.7:c.532G>C MANE Select	NP_005329.3:p.Val178Leu
NM_001243198.3:c.532G>C	NP_001230127.1:p.Val178Leu
NM_001382444.1:c.430G>C	NP_001369373.1:p.Val144Leu
NM_001382445.1:c.445G>C	NP_001369374.1:p.Val149Leu