Canonical Allele Identifier: CA399302784

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145846783
• MyVariant Identifiers: chr17:g.37880983C>G (hg19) ; chr17:g.39724730C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724730C>G , CM000679.2:g.39724730C>G	GRCh38
NC_000017.10:g.37880983C>G , CM000679.1:g.37880983C>G	GRCh37
NC_000017.9:g.35134509C>G	NCBI36
NG_007503.1:g.41591C>G , LRG_724:g.41591C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2312C>G MANE Select	ENSP00000269571.4:p.Ala771Gly
ENST00000269571.9:c.2312C>G	ENSP00000269571.4:p.Ala771Gly
ENST00000406381.6:c.2222C>G	ENSP00000385185.2:p.Ala741Gly
ENST00000445658.6:c.1484C>G	ENSP00000404047.2:p.Ala495Gly
ENST00000541774.5:c.2267C>G	ENSP00000446466.1:p.Ala756Gly
ENST00000578373.5:c.*2102C>G	ENSP00000463427.1:n.*2102C>G
ENST00000580074.1:c.418C>G
ENST00000583038.5:n.3446C>G
ENST00000584450.5:c.2312C>G	ENSP00000463714.1:p.Ala771Gly
ENST00000584601.5:c.2222C>G	ENSP00000462438.1:p.Ala741Gly
NM_001005862.2:c.2222C>G , LRG_724t1:c.2222C>G	NP_001005862.1:p.Ala741Gly
NM_001289936.1:c.2267C>G , LRG_724t4:c.2267C>G	NP_001276865.1:p.Ala756Gly
NM_001289937.1:c.2312C>G	NP_001276866.1:p.Ala771Gly
NM_004448.3:c.2312C>G , LRG_724t2:c.2312C>G	NP_004439.2:p.Ala771Gly
NR_110535.1:n.2636C>G
XM_024450641.1:c.2450C>G	XP_024306409.1:p.Ala817Gly
XM_024450642.1:c.2405C>G	XP_024306410.1:p.Ala802Gly
XM_024450643.1:c.2360C>G	XP_024306411.1:p.Ala787Gly
NM_001005862.3:c.2222C>G	NP_001005862.1:p.Ala741Gly
NM_001289936.2:c.2267C>G	NP_001276865.1:p.Ala756Gly
NM_001289937.2:c.2312C>G	NP_001276866.1:p.Ala771Gly
NM_001382782.1:c.2222C>G	NP_001369711.1:p.Ala741Gly
NM_001382783.1:c.2222C>G	NP_001369712.1:p.Ala741Gly
NM_001382784.1:c.2429C>G	NP_001369713.1:p.Ala810Gly
NM_001382785.1:c.2414C>G	NP_001369714.1:p.Ala805Gly
NM_001382786.1:c.2393C>G	NP_001369715.1:p.Ala798Gly
NM_001382787.1:c.2387C>G	NP_001369716.1:p.Ala796Gly
NM_001382788.1:c.2342C>G	NP_001369717.1:p.Ala781Gly
NM_001382789.1:c.2333C>G	NP_001369718.1:p.Ala778Gly
NM_001382790.1:c.2309C>G	NP_001369719.1:p.Ala770Gly
NM_001382791.1:c.2303C>G	NP_001369720.1:p.Ala768Gly
NM_001382792.1:c.2276C>G	NP_001369721.1:p.Ala759Gly
NM_001382793.1:c.2270C>G	NP_001369722.1:p.Ala757Gly
NM_001382794.1:c.2270C>G	NP_001369723.1:p.Ala757Gly
NM_001382795.1:c.2264C>G	NP_001369724.1:p.Ala755Gly
NM_001382796.1:c.2312C>G	NP_001369725.1:p.Ala771Gly
NM_001382797.1:c.2213C>G	NP_001369726.1:p.Ala738Gly
NM_001382798.1:c.2312C>G	NP_001369727.1:p.Ala771Gly
NM_001382799.1:c.2132C>G	NP_001369728.1:p.Ala711Gly
NM_001382800.1:c.2308-319C>G	NP_001369729.1:n.2308-319C>G
NM_001382801.1:c.2264C>G	NP_001369730.1:p.Ala755Gly
NM_001382802.1:c.2054C>G	NP_001369731.1:p.Ala685Gly
NM_001382803.1:c.2270C>G	NP_001369732.1:p.Ala757Gly
NM_001382804.1:c.1484C>G	NP_001369733.1:p.Ala495Gly
NM_001382805.1:c.2208+1070C>G	NP_001369734.1:n.2208+1070C>G
NM_001382806.1:c.1274C>G	NP_001369735.1:p.Ala425Gly
NM_004448.4:c.2312C>G MANE Select	NP_004439.2:p.Ala771Gly
NR_110535.2:n.2550C>G