Canonical Allele Identifier: CA652465229

Gene: HEY1

Linked Data

• COSMIC: COSN17078519

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.79764224dup , CM000670.2:g.79764224dup	GRCh38
NC_000008.10:g.80676459dup , CM000670.1:g.80676459dup	GRCh37
NC_000008.9:g.80839014dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000435063.4:n.1693dup
ENST00000354724.8:c.*967dup MANE Select	ENSP00000346761.3:n.*967dup
ENST00000435063.3:n.1682dup
ENST00000519075.2:n.3490dup
ENST00000521111.2:n.3194dup
ENST00000523531.2:n.2132dup
ENST00000523976.2:c.*967dup	ENSP00000429792.1:n.*967dup
ENST00000674160.1:c.*1622dup	ENSP00000501529.1:n.*1622dup
ENST00000674177.1:c.*1709dup	ENSP00000501471.1:n.*1709dup
ENST00000674295.1:c.*967dup	ENSP00000501320.1:n.*967dup
ENST00000674358.1:c.*967dup	ENSP00000501370.1:n.*967dup
ENST00000674418.1:c.*967dup	ENSP00000501342.1:n.*967dup
ENST00000674439.1:n.2110dup
ENST00000337919.9:c.*967dup	ENSP00000338272.5:n.*967dup
ENST00000354724.7:c.*967dup	ENSP00000346761.3:n.*967dup
NM_001040708.1:c.*967dup	NP_001035798.1:n.*967dup
NM_001282851.1:c.*967dup	NP_001269780.1:n.*967dup
NM_012258.3:c.*967dup	NP_036390.3:n.*967dup
NM_012258.4:c.*967dup MANE Select	NP_036390.3:n.*967dup
NM_001040708.2:c.*967dup	NP_001035798.1:n.*967dup
NM_001282851.2:c.*967dup	NP_001269780.1:n.*967dup