Canonical Allele Identifier: CA367727308

Gene: HIP1

Linked Data

• MyVariant Identifiers: chr7:g.75211451C>A (hg19) ; chr7:g.75582135C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75582135C>A , CM000669.2:g.75582135C>A	GRCh38
NC_000007.13:g.75211451C>A , CM000669.1:g.75211451C>A	GRCh37
NC_000007.12:g.75049387C>A	NCBI36
NG_023251.2:g.161827G>T
NG_023251.3:g.161827G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336926.11:c.482G>T MANE Select	ENSP00000336747.6:p.Gly161Val
ENST00000336926.10:c.482G>T	ENSP00000336747.6:p.Gly161Val
ENST00000420909.1:c.395G>T	ENSP00000414280.1:p.Gly132Val
ENST00000434438.6:c.482G>T	ENSP00000410300.2:p.Gly161Val
ENST00000616821.4:c.395G>T	ENSP00000484528.1:p.Gly132Val
NM_001243198.2:c.482G>T	NP_001230127.1:p.Gly161Val
NM_005338.6:c.482G>T	NP_005329.3:p.Gly161Val
XM_005250304.2:c.395G>T	XP_005250361.1:p.Gly132Val
XM_005250305.2:c.380G>T	XP_005250362.1:p.Gly127Val
XM_011516116.1:c.482G>T	XP_011514418.1:p.Gly161Val
XM_011516116.2:c.482G>T	XP_011514418.1:p.Gly161Val
XM_017012099.1:c.440G>T	XP_016867588.1:p.Gly147Val
NM_005338.7:c.482G>T MANE Select	NP_005329.3:p.Gly161Val
NM_001243198.3:c.482G>T	NP_001230127.1:p.Gly161Val
NM_001382444.1:c.380G>T	NP_001369373.1:p.Gly127Val
NM_001382445.1:c.395G>T	NP_001369374.1:p.Gly132Val