Canonical Allele Identifier: CA2038219487
Gene: ERBB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56088210G= , CM000674.2:g.56088210G= GRCh38
NC_000012.11:g.56481994G= , CM000674.1:g.56481994G= GRCh37
NC_000012.10:g.54768261G= NCBI36
NG_011529.1:g.13103G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682431.1:n.1033+48G=
ENST00000683018.1:c.697+48G= ENSP00000506822.1:n.697+48G=
ENST00000683059.1:c.697+48G= ENSP00000507402.1:n.697+48G=
ENST00000683164.1:c.697+48G= ENSP00000508051.1:n.697+48G=
ENST00000683653.1:n.828+48G=
ENST00000684500.1:n.1003+48G=
ENST00000267101.8:c.874+48G= MANE Select ENSP00000267101.4:n.874+48G=
ENST00000267101.7:c.874+48G= ENSP00000267101.3:n.874+48G=
ENST00000415288.6:c.697+48G= ENSP00000408340.2:n.697+48G=
ENST00000546748.1:n.339+48G=
ENST00000550869.5:c.25-6271G= ENSP00000448671.1:n.25-6271G=
ENST00000551085.5:c.874+48G= ENSP00000448483.1:n.874+48G=
ENST00000551242.5:c.874+48G= ENSP00000447510.1:n.874+48G=
NM_001982.3:c.874+48G= NP_001973.2:n.874+48G=
NM_001982.4:c.874+48G= MANE Select NP_001973.2:n.874+48G=