Canonical Allele Identifier: CA399303055

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881036T>G (hg19) ; chr17:g.39724783T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2365T>G MANE Select	ENSP00000269571.4:p.Cys789Gly
ENST00000269571.9:c.2365T>G	ENSP00000269571.4:p.Cys789Gly
ENST00000406381.6:c.2275T>G	ENSP00000385185.2:p.Cys759Gly
ENST00000445658.6:c.1537T>G	ENSP00000404047.2:p.Cys513Gly
ENST00000541774.5:c.2320T>G	ENSP00000446466.1:p.Cys774Gly
ENST00000578373.5:c.*2155T>G	ENSP00000463427.1:n.*2155T>G
ENST00000580074.1:c.471T>G
ENST00000583038.5:n.3499T>G
ENST00000584450.5:c.2365T>G	ENSP00000463714.1:p.Cys789Gly
ENST00000584601.5:c.2275T>G	ENSP00000462438.1:p.Cys759Gly
NM_001005862.2:c.2275T>G , LRG_724t1:c.2275T>G	NP_001005862.1:p.Cys759Gly
NM_001289936.1:c.2320T>G , LRG_724t4:c.2320T>G	NP_001276865.1:p.Cys774Gly
NM_001289937.1:c.2365T>G	NP_001276866.1:p.Cys789Gly
NM_004448.3:c.2365T>G , LRG_724t2:c.2365T>G	NP_004439.2:p.Cys789Gly
NR_110535.1:n.2689T>G
XM_024450641.1:c.2503T>G	XP_024306409.1:p.Cys835Gly
XM_024450642.1:c.2458T>G	XP_024306410.1:p.Cys820Gly
XM_024450643.1:c.2413T>G	XP_024306411.1:p.Cys805Gly
NM_001005862.3:c.2275T>G	NP_001005862.1:p.Cys759Gly
NM_001289936.2:c.2320T>G	NP_001276865.1:p.Cys774Gly
NM_001289937.2:c.2365T>G	NP_001276866.1:p.Cys789Gly
NM_001382782.1:c.2275T>G	NP_001369711.1:p.Cys759Gly
NM_001382783.1:c.2275T>G	NP_001369712.1:p.Cys759Gly
NM_001382784.1:c.2482T>G	NP_001369713.1:p.Cys828Gly
NM_001382785.1:c.2467T>G	NP_001369714.1:p.Cys823Gly
NM_001382786.1:c.2446T>G	NP_001369715.1:p.Cys816Gly
NM_001382787.1:c.2440T>G	NP_001369716.1:p.Cys814Gly
NM_001382788.1:c.2395T>G	NP_001369717.1:p.Cys799Gly
NM_001382789.1:c.2386T>G	NP_001369718.1:p.Cys796Gly
NM_001382790.1:c.2362T>G	NP_001369719.1:p.Cys788Gly
NM_001382791.1:c.2356T>G	NP_001369720.1:p.Cys786Gly
NM_001382792.1:c.2329T>G	NP_001369721.1:p.Cys777Gly
NM_001382793.1:c.2323T>G	NP_001369722.1:p.Cys775Gly
NM_001382794.1:c.2323T>G	NP_001369723.1:p.Cys775Gly
NM_001382795.1:c.2317T>G	NP_001369724.1:p.Cys773Gly
NM_001382796.1:c.2365T>G	NP_001369725.1:p.Cys789Gly
NM_001382797.1:c.2266T>G	NP_001369726.1:p.Cys756Gly
NM_001382798.1:c.2365T>G	NP_001369727.1:p.Cys789Gly
NM_001382799.1:c.2185T>G	NP_001369728.1:p.Cys729Gly
NM_001382800.1:c.2308-266T>G	NP_001369729.1:n.2308-266T>G
NM_001382801.1:c.2317T>G	NP_001369730.1:p.Cys773Gly
NM_001382802.1:c.2107T>G	NP_001369731.1:p.Cys703Gly
NM_001382803.1:c.2323T>G	NP_001369732.1:p.Cys775Gly
NM_001382804.1:c.1537T>G	NP_001369733.1:p.Cys513Gly
NM_001382805.1:c.2208+1123T>G	NP_001369734.1:n.2208+1123T>G
NM_001382806.1:c.1327T>G	NP_001369735.1:p.Cys443Gly
NM_004448.4:c.2365T>G MANE Select	NP_004439.2:p.Cys789Gly
NR_110535.2:n.2603T>G