Canonical Allele Identifier: CA399303423

Gene: ERBB2

Linked Data

• dbSNP Id: rs977391376
• MyVariant Identifiers: chr17:g.37881093G>T (hg19) ; chr17:g.39724840G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724840G>T , CM000679.2:g.39724840G>T	GRCh38
NC_000017.10:g.37881093G>T , CM000679.1:g.37881093G>T	GRCh37
NC_000017.9:g.35134619G>T	NCBI36
NG_007503.1:g.41701G>T , LRG_724:g.41701G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2422G>T MANE Select	ENSP00000269571.4:p.Asp808Tyr
ENST00000269571.9:c.2422G>T	ENSP00000269571.4:p.Asp808Tyr
ENST00000406381.6:c.2332G>T	ENSP00000385185.2:p.Asp778Tyr
ENST00000445658.6:c.1594G>T	ENSP00000404047.2:p.Asp532Tyr
ENST00000541774.5:c.2377G>T	ENSP00000446466.1:p.Asp793Tyr
ENST00000578373.5:c.*2212G>T	ENSP00000463427.1:n.*2212G>T
ENST00000580074.1:c.528G>T
ENST00000583038.5:n.3556G>T
ENST00000584450.5:c.2422G>T	ENSP00000463714.1:p.Asp808Tyr
ENST00000584601.5:c.2332G>T	ENSP00000462438.1:p.Asp778Tyr
NM_001005862.2:c.2332G>T , LRG_724t1:c.2332G>T	NP_001005862.1:p.Asp778Tyr
NM_001289936.1:c.2377G>T , LRG_724t4:c.2377G>T	NP_001276865.1:p.Asp793Tyr
NM_001289937.1:c.2422G>T	NP_001276866.1:p.Asp808Tyr
NM_004448.3:c.2422G>T , LRG_724t2:c.2422G>T	NP_004439.2:p.Asp808Tyr
NR_110535.1:n.2746G>T
XM_024450641.1:c.2560G>T	XP_024306409.1:p.Asp854Tyr
XM_024450642.1:c.2515G>T	XP_024306410.1:p.Asp839Tyr
XM_024450643.1:c.2470G>T	XP_024306411.1:p.Asp824Tyr
NM_001005862.3:c.2332G>T	NP_001005862.1:p.Asp778Tyr
NM_001289936.2:c.2377G>T	NP_001276865.1:p.Asp793Tyr
NM_001289937.2:c.2422G>T	NP_001276866.1:p.Asp808Tyr
NM_001382782.1:c.2332G>T	NP_001369711.1:p.Asp778Tyr
NM_001382783.1:c.2332G>T	NP_001369712.1:p.Asp778Tyr
NM_001382784.1:c.2539G>T	NP_001369713.1:p.Asp847Tyr
NM_001382785.1:c.2524G>T	NP_001369714.1:p.Asp842Tyr
NM_001382786.1:c.2503G>T	NP_001369715.1:p.Asp835Tyr
NM_001382787.1:c.2497G>T	NP_001369716.1:p.Asp833Tyr
NM_001382788.1:c.2452G>T	NP_001369717.1:p.Asp818Tyr
NM_001382789.1:c.2443G>T	NP_001369718.1:p.Asp815Tyr
NM_001382790.1:c.2419G>T	NP_001369719.1:p.Asp807Tyr
NM_001382791.1:c.2413G>T	NP_001369720.1:p.Asp805Tyr
NM_001382792.1:c.2386G>T	NP_001369721.1:p.Asp796Tyr
NM_001382793.1:c.2380G>T	NP_001369722.1:p.Asp794Tyr
NM_001382794.1:c.2380G>T	NP_001369723.1:p.Asp794Tyr
NM_001382795.1:c.2374G>T	NP_001369724.1:p.Asp792Tyr
NM_001382796.1:c.2422G>T	NP_001369725.1:p.Asp808Tyr
NM_001382797.1:c.2323G>T	NP_001369726.1:p.Asp775Tyr
NM_001382798.1:c.2422G>T	NP_001369727.1:p.Asp808Tyr
NM_001382799.1:c.2242G>T	NP_001369728.1:p.Asp748Tyr
NM_001382800.1:c.2308-209G>T	NP_001369729.1:n.2308-209G>T
NM_001382801.1:c.2374G>T	NP_001369730.1:p.Asp792Tyr
NM_001382802.1:c.2164G>T	NP_001369731.1:p.Asp722Tyr
NM_001382803.1:c.2380G>T	NP_001369732.1:p.Asp794Tyr
NM_001382804.1:c.1594G>T	NP_001369733.1:p.Asp532Tyr
NM_001382805.1:c.2208+1180G>T	NP_001369734.1:n.2208+1180G>T
NM_001382806.1:c.1384G>T	NP_001369735.1:p.Asp462Tyr
NM_004448.4:c.2422G>T MANE Select	NP_004439.2:p.Asp808Tyr
NR_110535.2:n.2660G>T