Canonical Allele Identifier: CA385291710

Gene: ERBB3

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56088823C>A , CM000674.2:g.56088823C>A	GRCh38
NC_000012.11:g.56482607C>A , CM000674.1:g.56482607C>A	GRCh37
NC_000012.10:g.54768874C>A	NCBI36
NG_011529.1:g.13716C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682431.1:n.1223C>A
ENST00000683018.1:c.887C>A	ENSP00000506822.1:p.Thr296Asn
ENST00000683059.1:c.887C>A	ENSP00000507402.1:p.Thr296Asn
ENST00000683164.1:c.887C>A	ENSP00000508051.1:p.Thr296Asn
ENST00000683653.1:n.1018C>A
ENST00000684500.1:n.1193C>A
ENST00000267101.8:c.1064C>A MANE Select	ENSP00000267101.4:p.Thr355Asn
ENST00000267101.7:c.1064C>A	ENSP00000267101.3:p.Thr355Asn
ENST00000415288.6:c.887C>A	ENSP00000408340.2:p.Thr296Asn
ENST00000546748.1:n.529C>A
ENST00000550869.5:c.25-5658C>A	ENSP00000448671.1:n.25-5658C>A
ENST00000551085.5:c.1064C>A	ENSP00000448483.1:p.Thr355Asn
ENST00000551176.1:n.104C>A
ENST00000551242.5:c.988+167C>A	ENSP00000447510.1:n.988+167C>A
NM_001982.3:c.1064C>A	NP_001973.2:p.Thr355Asn
NM_001982.4:c.1064C>A MANE Select	NP_001973.2:p.Thr355Asn