Canonical Allele Identifier: CA2038219111
Gene: ERBB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56087982A= , CM000674.2:g.56087982A= GRCh38
NC_000012.11:g.56481766A= , CM000674.1:g.56481766A= GRCh37
NC_000012.10:g.54768033A= NCBI36
NG_011529.1:g.12875A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682431.1:n.892-39A=
ENST00000683018.1:c.556-39A= ENSP00000506822.1:n.556-39A=
ENST00000683059.1:c.556-39A= ENSP00000507402.1:n.556-39A=
ENST00000683164.1:c.556-39A= ENSP00000508051.1:n.556-39A=
ENST00000683653.1:n.687-39A=
ENST00000684500.1:n.862-39A=
ENST00000267101.8:c.733-39A= MANE Select ENSP00000267101.4:n.733-39A=
ENST00000267101.7:c.733-39A= ENSP00000267101.3:n.733-39A=
ENST00000415288.6:c.556-39A= ENSP00000408340.2:n.556-39A=
ENST00000546748.1:n.159A=
ENST00000549472.1:n.476-39A=
ENST00000550869.5:c.25-6499A= ENSP00000448671.1:n.25-6499A=
ENST00000551085.5:c.733-39A= ENSP00000448483.1:n.733-39A=
ENST00000551242.5:c.733-39A= ENSP00000447510.1:n.733-39A=
NM_001982.3:c.733-39A= NP_001973.2:n.733-39A=
NM_001982.4:c.733-39A= MANE Select NP_001973.2:n.733-39A=