Canonical Allele Identifier: CA399314280

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059870846
• MyVariant Identifiers: chr17:g.37884181G>T (hg19) ; chr17:g.39727928G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727928G>T , CM000679.2:g.39727928G>T	GRCh38
NC_000017.10:g.37884181G>T , CM000679.1:g.37884181G>T	GRCh37
NC_000017.9:g.35137707G>T	NCBI36
NG_007503.1:g.44789G>T , LRG_724:g.44789G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3652G>T MANE Select	ENSP00000269571.4:p.Asp1218Tyr
ENST00000269571.9:c.3652G>T	ENSP00000269571.4:p.Asp1218Tyr
ENST00000406381.6:c.3562G>T	ENSP00000385185.2:p.Asp1188Tyr
ENST00000445658.6:c.2824G>T	ENSP00000404047.2:p.Asp942Tyr
ENST00000541774.5:c.3607G>T	ENSP00000446466.1:p.Asp1203Tyr
ENST00000578373.5:c.*3442G>T	ENSP00000463427.1:n.*3442G>T
ENST00000584450.5:c.*231G>T	ENSP00000463714.1:n.*231G>T
ENST00000584601.5:c.3562G>T	ENSP00000462438.1:p.Asp1188Tyr
NM_001005862.2:c.3562G>T , LRG_724t1:c.3562G>T	NP_001005862.1:p.Asp1188Tyr
NM_001289936.1:c.3607G>T , LRG_724t4:c.3607G>T	NP_001276865.1:p.Asp1203Tyr
NM_001289937.1:c.*231G>T	NP_001276866.1:n.*231G>T
NM_004448.3:c.3652G>T , LRG_724t2:c.3652G>T	NP_004439.2:p.Asp1218Tyr
NR_110535.1:n.3976G>T
XM_024450641.1:c.3790G>T	XP_024306409.1:p.Asp1264Tyr
XM_024450642.1:c.3745G>T	XP_024306410.1:p.Asp1249Tyr
XM_024450643.1:c.3700G>T	XP_024306411.1:p.Asp1234Tyr
NM_001005862.3:c.3562G>T	NP_001005862.1:p.Asp1188Tyr
NM_001289936.2:c.3607G>T	NP_001276865.1:p.Asp1203Tyr
NM_001289937.2:c.*231G>T	NP_001276866.1:n.*231G>T
NM_001382782.1:c.3562G>T	NP_001369711.1:p.Asp1188Tyr
NM_001382783.1:c.3562G>T	NP_001369712.1:p.Asp1188Tyr
NM_001382784.1:c.3769G>T	NP_001369713.1:p.Asp1257Tyr
NM_001382785.1:c.3754G>T	NP_001369714.1:p.Asp1252Tyr
NM_001382786.1:c.3733G>T	NP_001369715.1:p.Asp1245Tyr
NM_001382787.1:c.3727G>T	NP_001369716.1:p.Asp1243Tyr
NM_001382788.1:c.3682G>T	NP_001369717.1:p.Asp1228Tyr
NM_001382789.1:c.3673G>T	NP_001369718.1:p.Asp1225Tyr
NM_001382790.1:c.3649G>T	NP_001369719.1:p.Asp1217Tyr
NM_001382791.1:c.3643G>T	NP_001369720.1:p.Asp1215Tyr
NM_001382792.1:c.3616G>T	NP_001369721.1:p.Asp1206Tyr
NM_001382793.1:c.3610G>T	NP_001369722.1:p.Asp1204Tyr
NM_001382794.1:c.3610G>T	NP_001369723.1:p.Asp1204Tyr
NM_001382795.1:c.3604G>T	NP_001369724.1:p.Asp1202Tyr
NM_001382796.1:c.3565G>T	NP_001369725.1:p.Asp1189Tyr
NM_001382797.1:c.3553G>T	NP_001369726.1:p.Asp1185Tyr
NM_001382798.1:c.3496G>T	NP_001369727.1:p.Asp1166Tyr
NM_001382799.1:c.3472G>T	NP_001369728.1:p.Asp1158Tyr
NM_001382800.1:c.3466G>T	NP_001369729.1:p.Asp1156Tyr
NM_001382801.1:c.3448G>T	NP_001369730.1:p.Asp1150Tyr
NM_001382802.1:c.3394G>T	NP_001369731.1:p.Asp1132Tyr
NM_001382803.1:c.*231G>T	NP_001369732.1:n.*231G>T
NM_001382804.1:c.2824G>T	NP_001369733.1:p.Asp942Tyr
NM_001382805.1:c.2701G>T	NP_001369734.1:p.Asp901Tyr
NM_001382806.1:c.2614G>T	NP_001369735.1:p.Asp872Tyr
NM_004448.4:c.3652G>T MANE Select	NP_004439.2:p.Asp1218Tyr
NR_110535.2:n.3890G>T