Canonical Allele Identifier: CA2687704928

Gene: HEY1

Linked Data

• gnomAD v4: 8-79764326-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.79764326C>T , CM000670.2:g.79764326C>T	GRCh38
NC_000008.10:g.80676561C>T , CM000670.1:g.80676561C>T	GRCh37
NC_000008.9:g.80839116C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435063.4:n.1588G>A
ENST00000354724.8:c.*862G>A MANE Select	ENSP00000346761.3:n.*862G>A
ENST00000435063.3:n.1577G>A
ENST00000519075.2:n.3385G>A
ENST00000521111.2:n.3089G>A
ENST00000523531.2:n.2027G>A
ENST00000523976.2:c.*862G>A	ENSP00000429792.1:n.*862G>A
ENST00000674160.1:c.*1517G>A	ENSP00000501529.1:n.*1517G>A
ENST00000674177.1:c.*1604G>A	ENSP00000501471.1:n.*1604G>A
ENST00000674295.1:c.*862G>A	ENSP00000501320.1:n.*862G>A
ENST00000674358.1:c.*862G>A	ENSP00000501370.1:n.*862G>A
ENST00000674418.1:c.*862G>A	ENSP00000501342.1:n.*862G>A
ENST00000674439.1:n.2005G>A
ENST00000337919.9:c.*862G>A	ENSP00000338272.5:n.*862G>A
ENST00000354724.7:c.*862G>A	ENSP00000346761.3:n.*862G>A
NM_001040708.1:c.*862G>A	NP_001035798.1:n.*862G>A
NM_001282851.1:c.*862G>A	NP_001269780.1:n.*862G>A
NM_012258.3:c.*862G>A	NP_036390.3:n.*862G>A
NM_012258.4:c.*862G>A MANE Select	NP_036390.3:n.*862G>A
NM_001040708.2:c.*862G>A	NP_001035798.1:n.*862G>A
NM_001282851.2:c.*862G>A	NP_001269780.1:n.*862G>A