Canonical Allele Identifier: CA385287437

Gene: ERBB3

Linked Data

• MyVariant Identifiers: chr12:g.56481868A>G (hg19) ; chr12:g.56088084A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56088084A>G , CM000674.2:g.56088084A>G	GRCh38
NC_000012.11:g.56481868A>G , CM000674.1:g.56481868A>G	GRCh37
NC_000012.10:g.54768135A>G	NCBI36
NG_011529.1:g.12977A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682431.1:n.955A>G
ENST00000683018.1:c.619A>G	ENSP00000506822.1:p.Asn207Asp
ENST00000683059.1:c.619A>G	ENSP00000507402.1:p.Asn207Asp
ENST00000683164.1:c.619A>G	ENSP00000508051.1:p.Asn207Asp
ENST00000683653.1:n.750A>G
ENST00000684500.1:n.925A>G
ENST00000267101.8:c.796A>G MANE Select	ENSP00000267101.4:p.Asn266Asp
ENST00000267101.7:c.796A>G	ENSP00000267101.3:p.Asn266Asp
ENST00000415288.6:c.619A>G	ENSP00000408340.2:p.Asn207Asp
ENST00000546748.1:n.261A>G
ENST00000550869.5:c.25-6397A>G	ENSP00000448671.1:n.25-6397A>G
ENST00000551085.5:c.796A>G	ENSP00000448483.1:p.Asn266Asp
ENST00000551242.5:c.796A>G	ENSP00000447510.1:p.Asn266Asp
NM_001982.3:c.796A>G	NP_001973.2:p.Asn266Asp
NM_001982.4:c.796A>G MANE Select	NP_001973.2:p.Asn266Asp