Canonical Allele Identifier: CA399303354

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881084T>C (hg19) ; chr17:g.39724831T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724831T>C , CM000679.2:g.39724831T>C	GRCh38
NC_000017.10:g.37881084T>C , CM000679.1:g.37881084T>C	GRCh37
NC_000017.9:g.35134610T>C	NCBI36
NG_007503.1:g.41692T>C , LRG_724:g.41692T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2413T>C MANE Select	ENSP00000269571.4:p.Cys805Arg
ENST00000269571.9:c.2413T>C	ENSP00000269571.4:p.Cys805Arg
ENST00000406381.6:c.2323T>C	ENSP00000385185.2:p.Cys775Arg
ENST00000445658.6:c.1585T>C	ENSP00000404047.2:p.Cys529Arg
ENST00000541774.5:c.2368T>C	ENSP00000446466.1:p.Cys790Arg
ENST00000578373.5:c.*2203T>C	ENSP00000463427.1:n.*2203T>C
ENST00000580074.1:c.519T>C
ENST00000583038.5:n.3547T>C
ENST00000584450.5:c.2413T>C	ENSP00000463714.1:p.Cys805Arg
ENST00000584601.5:c.2323T>C	ENSP00000462438.1:p.Cys775Arg
NM_001005862.2:c.2323T>C , LRG_724t1:c.2323T>C	NP_001005862.1:p.Cys775Arg
NM_001289936.1:c.2368T>C , LRG_724t4:c.2368T>C	NP_001276865.1:p.Cys790Arg
NM_001289937.1:c.2413T>C	NP_001276866.1:p.Cys805Arg
NM_004448.3:c.2413T>C , LRG_724t2:c.2413T>C	NP_004439.2:p.Cys805Arg
NR_110535.1:n.2737T>C
XM_024450641.1:c.2551T>C	XP_024306409.1:p.Cys851Arg
XM_024450642.1:c.2506T>C	XP_024306410.1:p.Cys836Arg
XM_024450643.1:c.2461T>C	XP_024306411.1:p.Cys821Arg
NM_001005862.3:c.2323T>C	NP_001005862.1:p.Cys775Arg
NM_001289936.2:c.2368T>C	NP_001276865.1:p.Cys790Arg
NM_001289937.2:c.2413T>C	NP_001276866.1:p.Cys805Arg
NM_001382782.1:c.2323T>C	NP_001369711.1:p.Cys775Arg
NM_001382783.1:c.2323T>C	NP_001369712.1:p.Cys775Arg
NM_001382784.1:c.2530T>C	NP_001369713.1:p.Cys844Arg
NM_001382785.1:c.2515T>C	NP_001369714.1:p.Cys839Arg
NM_001382786.1:c.2494T>C	NP_001369715.1:p.Cys832Arg
NM_001382787.1:c.2488T>C	NP_001369716.1:p.Cys830Arg
NM_001382788.1:c.2443T>C	NP_001369717.1:p.Cys815Arg
NM_001382789.1:c.2434T>C	NP_001369718.1:p.Cys812Arg
NM_001382790.1:c.2410T>C	NP_001369719.1:p.Cys804Arg
NM_001382791.1:c.2404T>C	NP_001369720.1:p.Cys802Arg
NM_001382792.1:c.2377T>C	NP_001369721.1:p.Cys793Arg
NM_001382793.1:c.2371T>C	NP_001369722.1:p.Cys791Arg
NM_001382794.1:c.2371T>C	NP_001369723.1:p.Cys791Arg
NM_001382795.1:c.2365T>C	NP_001369724.1:p.Cys789Arg
NM_001382796.1:c.2413T>C	NP_001369725.1:p.Cys805Arg
NM_001382797.1:c.2314T>C	NP_001369726.1:p.Cys772Arg
NM_001382798.1:c.2413T>C	NP_001369727.1:p.Cys805Arg
NM_001382799.1:c.2233T>C	NP_001369728.1:p.Cys745Arg
NM_001382800.1:c.2308-218T>C	NP_001369729.1:n.2308-218T>C
NM_001382801.1:c.2365T>C	NP_001369730.1:p.Cys789Arg
NM_001382802.1:c.2155T>C	NP_001369731.1:p.Cys719Arg
NM_001382803.1:c.2371T>C	NP_001369732.1:p.Cys791Arg
NM_001382804.1:c.1585T>C	NP_001369733.1:p.Cys529Arg
NM_001382805.1:c.2208+1171T>C	NP_001369734.1:n.2208+1171T>C
NM_001382806.1:c.1375T>C	NP_001369735.1:p.Cys459Arg
NM_004448.4:c.2413T>C MANE Select	NP_004439.2:p.Cys805Arg
NR_110535.2:n.2651T>C