Canonical Allele Identifier: CA399302779

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145846677
• MyVariant Identifiers: chr17:g.37880982G>C (hg19) ; chr17:g.39724729G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724729G>C , CM000679.2:g.39724729G>C	GRCh38
NC_000017.10:g.37880982G>C , CM000679.1:g.37880982G>C	GRCh37
NC_000017.9:g.35134508G>C	NCBI36
NG_007503.1:g.41590G>C , LRG_724:g.41590G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2311G>C MANE Select	ENSP00000269571.4:p.Ala771Pro
ENST00000269571.9:c.2311G>C	ENSP00000269571.4:p.Ala771Pro
ENST00000406381.6:c.2221G>C	ENSP00000385185.2:p.Ala741Pro
ENST00000445658.6:c.1483G>C	ENSP00000404047.2:p.Ala495Pro
ENST00000541774.5:c.2266G>C	ENSP00000446466.1:p.Ala756Pro
ENST00000578373.5:c.*2101G>C	ENSP00000463427.1:n.*2101G>C
ENST00000580074.1:c.417G>C
ENST00000583038.5:n.3445G>C
ENST00000584450.5:c.2311G>C	ENSP00000463714.1:p.Ala771Pro
ENST00000584601.5:c.2221G>C	ENSP00000462438.1:p.Ala741Pro
NM_001005862.2:c.2221G>C , LRG_724t1:c.2221G>C	NP_001005862.1:p.Ala741Pro
NM_001289936.1:c.2266G>C , LRG_724t4:c.2266G>C	NP_001276865.1:p.Ala756Pro
NM_001289937.1:c.2311G>C	NP_001276866.1:p.Ala771Pro
NM_004448.3:c.2311G>C , LRG_724t2:c.2311G>C	NP_004439.2:p.Ala771Pro
NR_110535.1:n.2635G>C
XM_024450641.1:c.2449G>C	XP_024306409.1:p.Ala817Pro
XM_024450642.1:c.2404G>C	XP_024306410.1:p.Ala802Pro
XM_024450643.1:c.2359G>C	XP_024306411.1:p.Ala787Pro
NM_001005862.3:c.2221G>C	NP_001005862.1:p.Ala741Pro
NM_001289936.2:c.2266G>C	NP_001276865.1:p.Ala756Pro
NM_001289937.2:c.2311G>C	NP_001276866.1:p.Ala771Pro
NM_001382782.1:c.2221G>C	NP_001369711.1:p.Ala741Pro
NM_001382783.1:c.2221G>C	NP_001369712.1:p.Ala741Pro
NM_001382784.1:c.2428G>C	NP_001369713.1:p.Ala810Pro
NM_001382785.1:c.2413G>C	NP_001369714.1:p.Ala805Pro
NM_001382786.1:c.2392G>C	NP_001369715.1:p.Ala798Pro
NM_001382787.1:c.2386G>C	NP_001369716.1:p.Ala796Pro
NM_001382788.1:c.2341G>C	NP_001369717.1:p.Ala781Pro
NM_001382789.1:c.2332G>C	NP_001369718.1:p.Ala778Pro
NM_001382790.1:c.2308G>C	NP_001369719.1:p.Ala770Pro
NM_001382791.1:c.2302G>C	NP_001369720.1:p.Ala768Pro
NM_001382792.1:c.2275G>C	NP_001369721.1:p.Ala759Pro
NM_001382793.1:c.2269G>C	NP_001369722.1:p.Ala757Pro
NM_001382794.1:c.2269G>C	NP_001369723.1:p.Ala757Pro
NM_001382795.1:c.2263G>C	NP_001369724.1:p.Ala755Pro
NM_001382796.1:c.2311G>C	NP_001369725.1:p.Ala771Pro
NM_001382797.1:c.2212G>C	NP_001369726.1:p.Ala738Pro
NM_001382798.1:c.2311G>C	NP_001369727.1:p.Ala771Pro
NM_001382799.1:c.2131G>C	NP_001369728.1:p.Ala711Pro
NM_001382800.1:c.2308-320G>C	NP_001369729.1:n.2308-320G>C
NM_001382801.1:c.2263G>C	NP_001369730.1:p.Ala755Pro
NM_001382802.1:c.2053G>C	NP_001369731.1:p.Ala685Pro
NM_001382803.1:c.2269G>C	NP_001369732.1:p.Ala757Pro
NM_001382804.1:c.1483G>C	NP_001369733.1:p.Ala495Pro
NM_001382805.1:c.2208+1069G>C	NP_001369734.1:n.2208+1069G>C
NM_001382806.1:c.1273G>C	NP_001369735.1:p.Ala425Pro
NM_004448.4:c.2311G>C MANE Select	NP_004439.2:p.Ala771Pro
NR_110535.2:n.2549G>C