Canonical Allele Identifier: CA2038240622
Gene: ERBB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56096870C= , CM000674.2:g.56096870C= GRCh38
NC_000012.11:g.56490654C= , CM000674.1:g.56490654C= GRCh37
NC_000012.10:g.54776921C= NCBI36
NG_011529.1:g.21763C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682431.1:n.3760+24C=
ENST00000683018.1:c.2097+24C= ENSP00000506822.1:n.2097+24C=
ENST00000683059.1:c.2097+24C= ENSP00000507402.1:n.2097+24C=
ENST00000683164.1:c.2097+24C= ENSP00000508051.1:n.2097+24C=
ENST00000683653.1:n.3007+24C=
ENST00000684500.1:n.3315+24C=
ENST00000684766.1:n.517+24C=
ENST00000267101.8:c.2274+24C= MANE Select ENSP00000267101.4:n.2274+24C=
ENST00000267101.7:c.2274+24C= ENSP00000267101.3:n.2274+24C=
ENST00000415288.6:c.2097+24C= ENSP00000408340.2:n.2097+24C=
ENST00000550070.6:c.537+338C= ENSP00000448946.2:n.537+338C=
ENST00000551085.5:c.2274+24C= ENSP00000448483.1:n.2274+24C=
ENST00000551242.5:c.989-3312C= ENSP00000447510.1:n.989-3312C=
ENST00000553131.5:c.-4+24C= ENSP00000449129.1:n.-4+24C=
NM_001982.3:c.2274+24C= NP_001973.2:n.2274+24C=
NM_001982.4:c.2274+24C= MANE Select NP_001973.2:n.2274+24C=