Canonical Allele Identifier: CA367727478

Gene: HIP1

Linked Data

• MyVariant Identifiers: chr7:g.75211467T>C (hg19) ; chr7:g.75582151T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75582151T>C , CM000669.2:g.75582151T>C	GRCh38
NC_000007.13:g.75211467T>C , CM000669.1:g.75211467T>C	GRCh37
NC_000007.12:g.75049403T>C	NCBI36
NG_023251.2:g.161811A>G
NG_023251.3:g.161811A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336926.11:c.466A>G MANE Select	ENSP00000336747.6:p.Asn156Asp
ENST00000336926.10:c.466A>G	ENSP00000336747.6:p.Asn156Asp
ENST00000420909.1:c.379A>G	ENSP00000414280.1:p.Asn127Asp
ENST00000434438.6:c.466A>G	ENSP00000410300.2:p.Asn156Asp
ENST00000616821.4:c.379A>G	ENSP00000484528.1:p.Asn127Asp
NM_001243198.2:c.466A>G	NP_001230127.1:p.Asn156Asp
NM_005338.6:c.466A>G	NP_005329.3:p.Asn156Asp
XM_005250304.2:c.379A>G	XP_005250361.1:p.Asn127Asp
XM_005250305.2:c.364A>G	XP_005250362.1:p.Asn122Asp
XM_011516116.1:c.466A>G	XP_011514418.1:p.Asn156Asp
XM_011516116.2:c.466A>G	XP_011514418.1:p.Asn156Asp
XM_017012099.1:c.424A>G	XP_016867588.1:p.Asn142Asp
NM_005338.7:c.466A>G MANE Select	NP_005329.3:p.Asn156Asp
NM_001243198.3:c.466A>G	NP_001230127.1:p.Asn156Asp
NM_001382444.1:c.364A>G	NP_001369373.1:p.Asn122Asp
NM_001382445.1:c.379A>G	NP_001369374.1:p.Asn127Asp