Canonical Allele Identifier: CA499670832

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145847226
• MyVariant Identifiers: chr17:g.37880990G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724737G>A , CM000679.2:g.39724737G>A	GRCh38
NC_000017.10:g.37880990G>A , CM000679.1:g.37880990G>A	GRCh37
NC_000017.9:g.35134516G>A	NCBI36
NG_007503.1:g.41598G>A , LRG_724:g.41598G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2319G>A MANE Select	ENSP00000269571.4:p.Val773=
ENST00000269571.9:c.2319G>A	ENSP00000269571.4:p.Val773=
ENST00000406381.6:c.2229G>A	ENSP00000385185.2:p.Val743=
ENST00000445658.6:c.1491G>A	ENSP00000404047.2:p.Val497=
ENST00000541774.5:c.2274G>A	ENSP00000446466.1:p.Val758=
ENST00000578373.5:c.*2109G>A	ENSP00000463427.1:n.*2109G>A
ENST00000580074.1:c.425G>A
ENST00000583038.5:n.3453G>A
ENST00000584450.5:c.2319G>A	ENSP00000463714.1:p.Val773=
ENST00000584601.5:c.2229G>A	ENSP00000462438.1:p.Val743=
NM_001005862.2:c.2229G>A , LRG_724t1:c.2229G>A	NP_001005862.1:p.Val743=
NM_001289936.1:c.2274G>A , LRG_724t4:c.2274G>A	NP_001276865.1:p.Val758=
NM_001289937.1:c.2319G>A	NP_001276866.1:p.Val773=
NM_004448.3:c.2319G>A , LRG_724t2:c.2319G>A	NP_004439.2:p.Val773=
NR_110535.1:n.2643G>A
XM_024450641.1:c.2457G>A	XP_024306409.1:p.Val819=
XM_024450642.1:c.2412G>A	XP_024306410.1:p.Val804=
XM_024450643.1:c.2367G>A	XP_024306411.1:p.Val789=
NM_001005862.3:c.2229G>A	NP_001005862.1:p.Val743=
NM_001289936.2:c.2274G>A	NP_001276865.1:p.Val758=
NM_001289937.2:c.2319G>A	NP_001276866.1:p.Val773=
NM_001382782.1:c.2229G>A	NP_001369711.1:p.Val743=
NM_001382783.1:c.2229G>A	NP_001369712.1:p.Val743=
NM_001382784.1:c.2436G>A	NP_001369713.1:p.Val812=
NM_001382785.1:c.2421G>A	NP_001369714.1:p.Val807=
NM_001382786.1:c.2400G>A	NP_001369715.1:p.Val800=
NM_001382787.1:c.2394G>A	NP_001369716.1:p.Val798=
NM_001382788.1:c.2349G>A	NP_001369717.1:p.Val783=
NM_001382789.1:c.2340G>A	NP_001369718.1:p.Val780=
NM_001382790.1:c.2316G>A	NP_001369719.1:p.Val772=
NM_001382791.1:c.2310G>A	NP_001369720.1:p.Val770=
NM_001382792.1:c.2283G>A	NP_001369721.1:p.Val761=
NM_001382793.1:c.2277G>A	NP_001369722.1:p.Val759=
NM_001382794.1:c.2277G>A	NP_001369723.1:p.Val759=
NM_001382795.1:c.2271G>A	NP_001369724.1:p.Val757=
NM_001382796.1:c.2319G>A	NP_001369725.1:p.Val773=
NM_001382797.1:c.2220G>A	NP_001369726.1:p.Val740=
NM_001382798.1:c.2319G>A	NP_001369727.1:p.Val773=
NM_001382799.1:c.2139G>A	NP_001369728.1:p.Val713=
NM_001382800.1:c.2308-312G>A	NP_001369729.1:n.2308-312G>A
NM_001382801.1:c.2271G>A	NP_001369730.1:p.Val757=
NM_001382802.1:c.2061G>A	NP_001369731.1:p.Val687=
NM_001382803.1:c.2277G>A	NP_001369732.1:p.Val759=
NM_001382804.1:c.1491G>A	NP_001369733.1:p.Val497=
NM_001382805.1:c.2208+1077G>A	NP_001369734.1:n.2208+1077G>A
NM_001382806.1:c.1281G>A	NP_001369735.1:p.Val427=
NM_004448.4:c.2319G>A MANE Select	NP_004439.2:p.Val773=
NR_110535.2:n.2557G>A