Canonical Allele Identifier: CA455711939

Gene: HIP1

Linked Data

• dbSNP Id: rs781800614
• MyVariant Identifiers: chr7:g.75211515_75211516del (hg19) ; chr7:g.75582199_75582200del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75582200_75582201del , CM000669.2:g.75582200_75582201del	GRCh38
NC_000007.13:g.75211516_75211517del , CM000669.1:g.75211516_75211517del	GRCh37
NC_000007.12:g.75049452_75049453del	NCBI36
NG_023251.2:g.161762_161763del
NG_023251.3:g.161762_161763del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336926.11:c.466-49_466-48del MANE Select	ENSP00000336747.6:n.466-49_466-48del
ENST00000336926.10:c.466-49_466-48del	ENSP00000336747.6:n.466-49_466-48del
ENST00000420909.1:c.379-49_379-48del	ENSP00000414280.1:n.379-49_379-48del
ENST00000434438.6:c.466-49_466-48del	ENSP00000410300.2:n.466-49_466-48del
ENST00000616821.4:c.379-49_379-48del	ENSP00000484528.1:n.379-49_379-48del
NM_001243198.2:c.466-49_466-48del	NP_001230127.1:n.466-49_466-48del
NM_005338.6:c.466-49_466-48del	NP_005329.3:n.466-49_466-48del
XM_005250304.2:c.379-49_379-48del	XP_005250361.1:n.379-49_379-48del
XM_005250305.2:c.364-49_364-48del	XP_005250362.1:n.364-49_364-48del
XM_011516116.1:c.466-49_466-48del	XP_011514418.1:n.466-49_466-48del
XM_011516116.2:c.466-49_466-48del	XP_011514418.1:n.466-49_466-48del
XM_017012099.1:c.424-49_424-48del	XP_016867588.1:n.424-49_424-48del
NM_005338.7:c.466-49_466-48del MANE Select	NP_005329.3:n.466-49_466-48del
NM_001243198.3:c.466-49_466-48del	NP_001230127.1:n.466-49_466-48del
NM_001382444.1:c.364-49_364-48del	NP_001369373.1:n.364-49_364-48del
NM_001382445.1:c.379-49_379-48del	NP_001369374.1:n.379-49_379-48del