Canonical Allele Identifier: CA605512830

Gene: ERBB3

Linked Data

• dbSNP Id: rs1404206850
• gnomAD v2: 12-56482082-C-CA
• gnomAD v3: 12-56088298-C-CA
• gnomAD v4: 12-56088298-C-CA
• MyVariant Identifiers: chr12:g.56482082_56482083insA (hg19) ; chr12:g.56088298_56088299insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56088299dup , CM000674.2:g.56088299dup	GRCh38
NC_000012.11:g.56482083dup , CM000674.1:g.56482083dup	GRCh37
NC_000012.10:g.54768350dup	NCBI36
NG_011529.1:g.13192dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682431.1:n.1033+137dup
ENST00000683018.1:c.697+137dup	ENSP00000506822.1:n.697+137dup
ENST00000683059.1:c.697+137dup	ENSP00000507402.1:n.697+137dup
ENST00000683164.1:c.697+137dup	ENSP00000508051.1:n.697+137dup
ENST00000683653.1:n.828+137dup
ENST00000684500.1:n.1003+137dup
ENST00000267101.8:c.874+137dup MANE Select	ENSP00000267101.4:n.874+137dup
ENST00000267101.7:c.874+137dup	ENSP00000267101.3:n.874+137dup
ENST00000415288.6:c.697+137dup	ENSP00000408340.2:n.697+137dup
ENST00000546748.1:n.339+137dup
ENST00000550869.5:c.25-6182dup	ENSP00000448671.1:n.25-6182dup
ENST00000551085.5:c.874+137dup	ENSP00000448483.1:n.874+137dup
ENST00000551242.5:c.874+137dup	ENSP00000447510.1:n.874+137dup
NM_001982.3:c.874+137dup	NP_001973.2:n.874+137dup
NM_001982.4:c.874+137dup MANE Select	NP_001973.2:n.874+137dup