Canonical Allele Identifier: CA2780986921

Gene: HEY1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.79764295T>A , CM000670.2:g.79764295T>A	GRCh38
NC_000008.10:g.80676530T>A , CM000670.1:g.80676530T>A	GRCh37
NC_000008.9:g.80839085T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000435063.4:n.1619A>T
ENST00000354724.8:c.*893A>T MANE Select	ENSP00000346761.3:n.*893A>T
ENST00000435063.3:n.1608A>T
ENST00000519075.2:n.3416A>T
ENST00000521111.2:n.3120A>T
ENST00000523531.2:n.2058A>T
ENST00000523976.2:c.*893A>T	ENSP00000429792.1:n.*893A>T
ENST00000674160.1:c.*1548A>T	ENSP00000501529.1:n.*1548A>T
ENST00000674177.1:c.*1635A>T	ENSP00000501471.1:n.*1635A>T
ENST00000674295.1:c.*893A>T	ENSP00000501320.1:n.*893A>T
ENST00000674358.1:c.*893A>T	ENSP00000501370.1:n.*893A>T
ENST00000674418.1:c.*893A>T	ENSP00000501342.1:n.*893A>T
ENST00000674439.1:n.2036A>T
ENST00000337919.9:c.*893A>T	ENSP00000338272.5:n.*893A>T
ENST00000354724.7:c.*893A>T	ENSP00000346761.3:n.*893A>T
NM_001040708.1:c.*893A>T	NP_001035798.1:n.*893A>T
NM_001282851.1:c.*893A>T	NP_001269780.1:n.*893A>T
NM_012258.3:c.*893A>T	NP_036390.3:n.*893A>T
NM_012258.4:c.*893A>T MANE Select	NP_036390.3:n.*893A>T
NM_001040708.2:c.*893A>T	NP_001035798.1:n.*893A>T
NM_001282851.2:c.*893A>T	NP_001269780.1:n.*893A>T