Canonical Allele Identifier: CA6622075

Gene: ERBB3

Linked Data

• dbSNP Id: rs768003972
• ExAC: 12:56481865 TACA / T
• gnomAD v2: 12-56481865-TACA-T
• gnomAD v4: 12-56088081-TACA-T
• MyVariant Identifiers: chr12:g.56481866_56481868del (hg19) ; chr12:g.56088082_56088084del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56088086_56088088del , CM000674.2:g.56088086_56088088del	GRCh38
NC_000012.11:g.56481870_56481872del , CM000674.1:g.56481870_56481872del	GRCh37
NC_000012.10:g.54768137_54768139del	NCBI36
NG_011529.1:g.12979_12981del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682431.1:n.957_959del
ENST00000683018.1:c.621_623del	ENSP00000506822.1:p.Asn207del
ENST00000683059.1:c.621_623del	ENSP00000507402.1:p.Asn207del
ENST00000683164.1:c.621_623del	ENSP00000508051.1:p.Asn207del
ENST00000683653.1:n.752_754del
ENST00000684500.1:n.927_929del
ENST00000267101.8:c.798_800del MANE Select	ENSP00000267101.4:p.Asn266del
ENST00000267101.7:c.798_800del	ENSP00000267101.3:p.Asn266del
ENST00000415288.6:c.621_623del	ENSP00000408340.2:p.Asn207del
ENST00000546748.1:n.263_265del
ENST00000550869.5:c.25-6395_25-6393del	ENSP00000448671.1:n.25-6395_25-6393del
ENST00000551085.5:c.798_800del	ENSP00000448483.1:p.Asn266del
ENST00000551242.5:c.798_800del	ENSP00000447510.1:p.Asn266del
NM_001982.3:c.798_800del	NP_001973.2:p.Asn266del
NM_001982.4:c.798_800del MANE Select	NP_001973.2:p.Asn266del