Canonical Allele Identifier: CA2776533417

Gene: HIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75582172G>C , CM000669.2:g.75582172G>C	GRCh38
NC_000007.13:g.75211488G>C , CM000669.1:g.75211488G>C	GRCh37
NC_000007.12:g.75049424G>C	NCBI36
NG_023251.2:g.161790C>G
NG_023251.3:g.161790C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336926.11:c.466-21C>G MANE Select	ENSP00000336747.6:n.466-21C>G
ENST00000336926.10:c.466-21C>G	ENSP00000336747.6:n.466-21C>G
ENST00000420909.1:c.379-21C>G	ENSP00000414280.1:n.379-21C>G
ENST00000434438.6:c.466-21C>G	ENSP00000410300.2:n.466-21C>G
ENST00000616821.4:c.379-21C>G	ENSP00000484528.1:n.379-21C>G
NM_001243198.2:c.466-21C>G	NP_001230127.1:n.466-21C>G
NM_005338.6:c.466-21C>G	NP_005329.3:n.466-21C>G
XM_005250304.2:c.379-21C>G	XP_005250361.1:n.379-21C>G
XM_005250305.2:c.364-21C>G	XP_005250362.1:n.364-21C>G
XM_011516116.1:c.466-21C>G	XP_011514418.1:n.466-21C>G
XM_011516116.2:c.466-21C>G	XP_011514418.1:n.466-21C>G
XM_017012099.1:c.424-21C>G	XP_016867588.1:n.424-21C>G
NM_005338.7:c.466-21C>G MANE Select	NP_005329.3:n.466-21C>G
NM_001243198.3:c.466-21C>G	NP_001230127.1:n.466-21C>G
NM_001382444.1:c.364-21C>G	NP_001369373.1:n.364-21C>G
NM_001382445.1:c.379-21C>G	NP_001369374.1:n.379-21C>G