Canonical Allele Identifier: CA399303063

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881037G>T (hg19) ; chr17:g.39724784G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724784G>T , CM000679.2:g.39724784G>T	GRCh38
NC_000017.10:g.37881037G>T , CM000679.1:g.37881037G>T	GRCh37
NC_000017.9:g.35134563G>T	NCBI36
NG_007503.1:g.41645G>T , LRG_724:g.41645G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2366G>T MANE Select	ENSP00000269571.4:p.Cys789Phe
ENST00000269571.9:c.2366G>T	ENSP00000269571.4:p.Cys789Phe
ENST00000406381.6:c.2276G>T	ENSP00000385185.2:p.Cys759Phe
ENST00000445658.6:c.1538G>T	ENSP00000404047.2:p.Cys513Phe
ENST00000541774.5:c.2321G>T	ENSP00000446466.1:p.Cys774Phe
ENST00000578373.5:c.*2156G>T	ENSP00000463427.1:n.*2156G>T
ENST00000580074.1:c.472G>T
ENST00000583038.5:n.3500G>T
ENST00000584450.5:c.2366G>T	ENSP00000463714.1:p.Cys789Phe
ENST00000584601.5:c.2276G>T	ENSP00000462438.1:p.Cys759Phe
NM_001005862.2:c.2276G>T , LRG_724t1:c.2276G>T	NP_001005862.1:p.Cys759Phe
NM_001289936.1:c.2321G>T , LRG_724t4:c.2321G>T	NP_001276865.1:p.Cys774Phe
NM_001289937.1:c.2366G>T	NP_001276866.1:p.Cys789Phe
NM_004448.3:c.2366G>T , LRG_724t2:c.2366G>T	NP_004439.2:p.Cys789Phe
NR_110535.1:n.2690G>T
XM_024450641.1:c.2504G>T	XP_024306409.1:p.Cys835Phe
XM_024450642.1:c.2459G>T	XP_024306410.1:p.Cys820Phe
XM_024450643.1:c.2414G>T	XP_024306411.1:p.Cys805Phe
NM_001005862.3:c.2276G>T	NP_001005862.1:p.Cys759Phe
NM_001289936.2:c.2321G>T	NP_001276865.1:p.Cys774Phe
NM_001289937.2:c.2366G>T	NP_001276866.1:p.Cys789Phe
NM_001382782.1:c.2276G>T	NP_001369711.1:p.Cys759Phe
NM_001382783.1:c.2276G>T	NP_001369712.1:p.Cys759Phe
NM_001382784.1:c.2483G>T	NP_001369713.1:p.Cys828Phe
NM_001382785.1:c.2468G>T	NP_001369714.1:p.Cys823Phe
NM_001382786.1:c.2447G>T	NP_001369715.1:p.Cys816Phe
NM_001382787.1:c.2441G>T	NP_001369716.1:p.Cys814Phe
NM_001382788.1:c.2396G>T	NP_001369717.1:p.Cys799Phe
NM_001382789.1:c.2387G>T	NP_001369718.1:p.Cys796Phe
NM_001382790.1:c.2363G>T	NP_001369719.1:p.Cys788Phe
NM_001382791.1:c.2357G>T	NP_001369720.1:p.Cys786Phe
NM_001382792.1:c.2330G>T	NP_001369721.1:p.Cys777Phe
NM_001382793.1:c.2324G>T	NP_001369722.1:p.Cys775Phe
NM_001382794.1:c.2324G>T	NP_001369723.1:p.Cys775Phe
NM_001382795.1:c.2318G>T	NP_001369724.1:p.Cys773Phe
NM_001382796.1:c.2366G>T	NP_001369725.1:p.Cys789Phe
NM_001382797.1:c.2267G>T	NP_001369726.1:p.Cys756Phe
NM_001382798.1:c.2366G>T	NP_001369727.1:p.Cys789Phe
NM_001382799.1:c.2186G>T	NP_001369728.1:p.Cys729Phe
NM_001382800.1:c.2308-265G>T	NP_001369729.1:n.2308-265G>T
NM_001382801.1:c.2318G>T	NP_001369730.1:p.Cys773Phe
NM_001382802.1:c.2108G>T	NP_001369731.1:p.Cys703Phe
NM_001382803.1:c.2324G>T	NP_001369732.1:p.Cys775Phe
NM_001382804.1:c.1538G>T	NP_001369733.1:p.Cys513Phe
NM_001382805.1:c.2208+1124G>T	NP_001369734.1:n.2208+1124G>T
NM_001382806.1:c.1328G>T	NP_001369735.1:p.Cys443Phe
NM_004448.4:c.2366G>T MANE Select	NP_004439.2:p.Cys789Phe
NR_110535.2:n.2604G>T