Canonical Allele Identifier: CA1796654139

Gene: HEY1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.79764308C= , CM000670.2:g.79764308C=	GRCh38
NC_000008.10:g.80676543C= , CM000670.1:g.80676543C=	GRCh37
NC_000008.9:g.80839098C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000435063.4:n.1606G=
ENST00000354724.8:c.*880G= MANE Select	ENSP00000346761.3:n.*880G=
ENST00000435063.3:n.1595G=
ENST00000519075.2:n.3403G=
ENST00000521111.2:n.3107G=
ENST00000523531.2:n.2045G=
ENST00000523976.2:c.*880G=	ENSP00000429792.1:n.*880G=
ENST00000674160.1:c.*1535G=	ENSP00000501529.1:n.*1535G=
ENST00000674177.1:c.*1622G=	ENSP00000501471.1:n.*1622G=
ENST00000674295.1:c.*880G=	ENSP00000501320.1:n.*880G=
ENST00000674358.1:c.*880G=	ENSP00000501370.1:n.*880G=
ENST00000674418.1:c.*880G=	ENSP00000501342.1:n.*880G=
ENST00000674439.1:n.2023G=
ENST00000337919.9:c.*880G=	ENSP00000338272.5:n.*880G=
ENST00000354724.7:c.*880G=	ENSP00000346761.3:n.*880G=
NM_001040708.1:c.*880G=	NP_001035798.1:n.*880G=
NM_001282851.1:c.*880G=	NP_001269780.1:n.*880G=
NM_012258.3:c.*880G=	NP_036390.3:n.*880G=
NM_012258.4:c.*880G= MANE Select	NP_036390.3:n.*880G=
NM_001040708.2:c.*880G=	NP_001035798.1:n.*880G=
NM_001282851.2:c.*880G=	NP_001269780.1:n.*880G=