Canonical Allele Identifier: CA385316342

Gene: ERBB3

Linked Data

• MyVariant Identifiers: chr12:g.56492652G>T (hg19) ; chr12:g.56098868G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56098868G>T , CM000674.2:g.56098868G>T	GRCh38
NC_000012.11:g.56492652G>T , CM000674.1:g.56492652G>T	GRCh37
NC_000012.10:g.54778919G>T	NCBI36
NG_011529.1:g.23761G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682431.1:n.4288G>T
ENST00000682512.1:n.1143G>T
ENST00000683018.1:c.2625G>T	ENSP00000506822.1:p.Gln875His
ENST00000683059.1:c.2625G>T	ENSP00000507402.1:p.Gln875His
ENST00000683142.1:n.406G>T
ENST00000683164.1:c.2625G>T	ENSP00000508051.1:p.Gln875His
ENST00000683653.1:n.3535G>T
ENST00000684500.1:n.3843G>T
ENST00000684766.1:n.1414-780G>T
ENST00000267101.8:c.2802G>T MANE Select	ENSP00000267101.4:p.Gln934His
ENST00000267101.7:c.2802G>T	ENSP00000267101.3:p.Gln934His
ENST00000415288.6:c.2625G>T	ENSP00000408340.2:p.Gln875His
ENST00000548709.1:n.439G>T
ENST00000549832.1:c.162G>T	ENSP00000448729.1:p.Gln54His
ENST00000550070.6:c.723G>T	ENSP00000448946.2:p.Gln241His
ENST00000551085.5:c.*219G>T	ENSP00000448483.1:n.*219G>T
ENST00000551242.5:c.989-1314G>T	ENSP00000447510.1:n.989-1314G>T
ENST00000553131.5:c.525G>T	ENSP00000449129.1:p.Gln175His
NM_001982.3:c.2802G>T	NP_001973.2:p.Gln934His
NM_001982.4:c.2802G>T MANE Select	NP_001973.2:p.Gln934His