Canonical Allele Identifier: CA399303712

Gene: ERBB2

Linked Data

• COSMIC: COSM116059
• MyVariant Identifiers: chr17:g.37881132G>T (hg19) ; chr17:g.39724879G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724879G>T , CM000679.2:g.39724879G>T	GRCh38
NC_000017.10:g.37881132G>T , CM000679.1:g.37881132G>T	GRCh37
NC_000017.9:g.35134658G>T	NCBI36
NG_007503.1:g.41740G>T , LRG_724:g.41740G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2461G>T MANE Select	ENSP00000269571.4:p.Asp821Tyr
ENST00000269571.9:c.2461G>T	ENSP00000269571.4:p.Asp821Tyr
ENST00000406381.6:c.2371G>T	ENSP00000385185.2:p.Asp791Tyr
ENST00000445658.6:c.1633G>T	ENSP00000404047.2:p.Asp545Tyr
ENST00000541774.5:c.2416G>T	ENSP00000446466.1:p.Asp806Tyr
ENST00000578373.5:c.*2251G>T	ENSP00000463427.1:n.*2251G>T
ENST00000580074.1:c.567G>T
ENST00000583038.5:n.3595G>T
ENST00000584450.5:c.2461G>T	ENSP00000463714.1:p.Asp821Tyr
ENST00000584601.5:c.2371G>T	ENSP00000462438.1:p.Asp791Tyr
NM_001005862.2:c.2371G>T , LRG_724t1:c.2371G>T	NP_001005862.1:p.Asp791Tyr
NM_001289936.1:c.2416G>T , LRG_724t4:c.2416G>T	NP_001276865.1:p.Asp806Tyr
NM_001289937.1:c.2461G>T	NP_001276866.1:p.Asp821Tyr
NM_004448.3:c.2461G>T , LRG_724t2:c.2461G>T	NP_004439.2:p.Asp821Tyr
NR_110535.1:n.2785G>T
XM_024450641.1:c.2599G>T	XP_024306409.1:p.Asp867Tyr
XM_024450642.1:c.2554G>T	XP_024306410.1:p.Asp852Tyr
XM_024450643.1:c.2509G>T	XP_024306411.1:p.Asp837Tyr
NM_001005862.3:c.2371G>T	NP_001005862.1:p.Asp791Tyr
NM_001289936.2:c.2416G>T	NP_001276865.1:p.Asp806Tyr
NM_001289937.2:c.2461G>T	NP_001276866.1:p.Asp821Tyr
NM_001382782.1:c.2371G>T	NP_001369711.1:p.Asp791Tyr
NM_001382783.1:c.2371G>T	NP_001369712.1:p.Asp791Tyr
NM_001382784.1:c.2578G>T	NP_001369713.1:p.Asp860Tyr
NM_001382785.1:c.2563G>T	NP_001369714.1:p.Asp855Tyr
NM_001382786.1:c.2542G>T	NP_001369715.1:p.Asp848Tyr
NM_001382787.1:c.2536G>T	NP_001369716.1:p.Asp846Tyr
NM_001382788.1:c.2491G>T	NP_001369717.1:p.Asp831Tyr
NM_001382789.1:c.2482G>T	NP_001369718.1:p.Asp828Tyr
NM_001382790.1:c.2458G>T	NP_001369719.1:p.Asp820Tyr
NM_001382791.1:c.2452G>T	NP_001369720.1:p.Asp818Tyr
NM_001382792.1:c.2425G>T	NP_001369721.1:p.Asp809Tyr
NM_001382793.1:c.2419G>T	NP_001369722.1:p.Asp807Tyr
NM_001382794.1:c.2419G>T	NP_001369723.1:p.Asp807Tyr
NM_001382795.1:c.2413G>T	NP_001369724.1:p.Asp805Tyr
NM_001382796.1:c.2461G>T	NP_001369725.1:p.Asp821Tyr
NM_001382797.1:c.2362G>T	NP_001369726.1:p.Asp788Tyr
NM_001382798.1:c.2461G>T	NP_001369727.1:p.Asp821Tyr
NM_001382799.1:c.2281G>T	NP_001369728.1:p.Asp761Tyr
NM_001382800.1:c.2308-170G>T	NP_001369729.1:n.2308-170G>T
NM_001382801.1:c.2413G>T	NP_001369730.1:p.Asp805Tyr
NM_001382802.1:c.2203G>T	NP_001369731.1:p.Asp735Tyr
NM_001382803.1:c.2419G>T	NP_001369732.1:p.Asp807Tyr
NM_001382804.1:c.1633G>T	NP_001369733.1:p.Asp545Tyr
NM_001382805.1:c.2208+1219G>T	NP_001369734.1:n.2208+1219G>T
NM_001382806.1:c.1423G>T	NP_001369735.1:p.Asp475Tyr
NM_004448.4:c.2461G>T MANE Select	NP_004439.2:p.Asp821Tyr
NR_110535.2:n.2699G>T