Canonical Allele Identifier: CA1796654129

Gene: HEY1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.79764297C= , CM000670.2:g.79764297C=	GRCh38
NC_000008.10:g.80676532C= , CM000670.1:g.80676532C=	GRCh37
NC_000008.9:g.80839087C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435063.4:n.1617G=
ENST00000354724.8:c.*891G= MANE Select	ENSP00000346761.3:n.*891G=
ENST00000435063.3:n.1606G=
ENST00000519075.2:n.3414G=
ENST00000521111.2:n.3118G=
ENST00000523531.2:n.2056G=
ENST00000523976.2:c.*891G=	ENSP00000429792.1:n.*891G=
ENST00000674160.1:c.*1546G=	ENSP00000501529.1:n.*1546G=
ENST00000674177.1:c.*1633G=	ENSP00000501471.1:n.*1633G=
ENST00000674295.1:c.*891G=	ENSP00000501320.1:n.*891G=
ENST00000674358.1:c.*891G=	ENSP00000501370.1:n.*891G=
ENST00000674418.1:c.*891G=	ENSP00000501342.1:n.*891G=
ENST00000674439.1:n.2034G=
ENST00000337919.9:c.*891G=	ENSP00000338272.5:n.*891G=
ENST00000354724.7:c.*891G=	ENSP00000346761.3:n.*891G=
NM_001040708.1:c.*891G=	NP_001035798.1:n.*891G=
NM_001282851.1:c.*891G=	NP_001269780.1:n.*891G=
NM_012258.3:c.*891G=	NP_036390.3:n.*891G=
NM_012258.4:c.*891G= MANE Select	NP_036390.3:n.*891G=
NM_001040708.2:c.*891G=	NP_001035798.1:n.*891G=
NM_001282851.2:c.*891G=	NP_001269780.1:n.*891G=