Canonical Allele Identifier: CA399303052

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145849346
• MyVariant Identifiers: chr17:g.37881036T>A (hg19) ; chr17:g.39724783T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724783T>A , CM000679.2:g.39724783T>A	GRCh38
NC_000017.10:g.37881036T>A , CM000679.1:g.37881036T>A	GRCh37
NC_000017.9:g.35134562T>A	NCBI36
NG_007503.1:g.41644T>A , LRG_724:g.41644T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2365T>A MANE Select	ENSP00000269571.4:p.Cys789Ser
ENST00000269571.9:c.2365T>A	ENSP00000269571.4:p.Cys789Ser
ENST00000406381.6:c.2275T>A	ENSP00000385185.2:p.Cys759Ser
ENST00000445658.6:c.1537T>A	ENSP00000404047.2:p.Cys513Ser
ENST00000541774.5:c.2320T>A	ENSP00000446466.1:p.Cys774Ser
ENST00000578373.5:c.*2155T>A	ENSP00000463427.1:n.*2155T>A
ENST00000580074.1:c.471T>A
ENST00000583038.5:n.3499T>A
ENST00000584450.5:c.2365T>A	ENSP00000463714.1:p.Cys789Ser
ENST00000584601.5:c.2275T>A	ENSP00000462438.1:p.Cys759Ser
NM_001005862.2:c.2275T>A , LRG_724t1:c.2275T>A	NP_001005862.1:p.Cys759Ser
NM_001289936.1:c.2320T>A , LRG_724t4:c.2320T>A	NP_001276865.1:p.Cys774Ser
NM_001289937.1:c.2365T>A	NP_001276866.1:p.Cys789Ser
NM_004448.3:c.2365T>A , LRG_724t2:c.2365T>A	NP_004439.2:p.Cys789Ser
NR_110535.1:n.2689T>A
XM_024450641.1:c.2503T>A	XP_024306409.1:p.Cys835Ser
XM_024450642.1:c.2458T>A	XP_024306410.1:p.Cys820Ser
XM_024450643.1:c.2413T>A	XP_024306411.1:p.Cys805Ser
NM_001005862.3:c.2275T>A	NP_001005862.1:p.Cys759Ser
NM_001289936.2:c.2320T>A	NP_001276865.1:p.Cys774Ser
NM_001289937.2:c.2365T>A	NP_001276866.1:p.Cys789Ser
NM_001382782.1:c.2275T>A	NP_001369711.1:p.Cys759Ser
NM_001382783.1:c.2275T>A	NP_001369712.1:p.Cys759Ser
NM_001382784.1:c.2482T>A	NP_001369713.1:p.Cys828Ser
NM_001382785.1:c.2467T>A	NP_001369714.1:p.Cys823Ser
NM_001382786.1:c.2446T>A	NP_001369715.1:p.Cys816Ser
NM_001382787.1:c.2440T>A	NP_001369716.1:p.Cys814Ser
NM_001382788.1:c.2395T>A	NP_001369717.1:p.Cys799Ser
NM_001382789.1:c.2386T>A	NP_001369718.1:p.Cys796Ser
NM_001382790.1:c.2362T>A	NP_001369719.1:p.Cys788Ser
NM_001382791.1:c.2356T>A	NP_001369720.1:p.Cys786Ser
NM_001382792.1:c.2329T>A	NP_001369721.1:p.Cys777Ser
NM_001382793.1:c.2323T>A	NP_001369722.1:p.Cys775Ser
NM_001382794.1:c.2323T>A	NP_001369723.1:p.Cys775Ser
NM_001382795.1:c.2317T>A	NP_001369724.1:p.Cys773Ser
NM_001382796.1:c.2365T>A	NP_001369725.1:p.Cys789Ser
NM_001382797.1:c.2266T>A	NP_001369726.1:p.Cys756Ser
NM_001382798.1:c.2365T>A	NP_001369727.1:p.Cys789Ser
NM_001382799.1:c.2185T>A	NP_001369728.1:p.Cys729Ser
NM_001382800.1:c.2308-266T>A	NP_001369729.1:n.2308-266T>A
NM_001382801.1:c.2317T>A	NP_001369730.1:p.Cys773Ser
NM_001382802.1:c.2107T>A	NP_001369731.1:p.Cys703Ser
NM_001382803.1:c.2323T>A	NP_001369732.1:p.Cys775Ser
NM_001382804.1:c.1537T>A	NP_001369733.1:p.Cys513Ser
NM_001382805.1:c.2208+1123T>A	NP_001369734.1:n.2208+1123T>A
NM_001382806.1:c.1327T>A	NP_001369735.1:p.Cys443Ser
NM_004448.4:c.2365T>A MANE Select	NP_004439.2:p.Cys789Ser
NR_110535.2:n.2603T>A