Canonical Allele Identifier: CA399314292

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143312211
• MyVariant Identifiers: chr17:g.37884182A>T (hg19) ; chr17:g.39727929A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727929A>T , CM000679.2:g.39727929A>T	GRCh38
NC_000017.10:g.37884182A>T , CM000679.1:g.37884182A>T	GRCh37
NC_000017.9:g.35137708A>T	NCBI36
NG_007503.1:g.44790A>T , LRG_724:g.44790A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3653A>T MANE Select	ENSP00000269571.4:p.Asp1218Val
ENST00000269571.9:c.3653A>T	ENSP00000269571.4:p.Asp1218Val
ENST00000406381.6:c.3563A>T	ENSP00000385185.2:p.Asp1188Val
ENST00000445658.6:c.2825A>T	ENSP00000404047.2:p.Asp942Val
ENST00000541774.5:c.3608A>T	ENSP00000446466.1:p.Asp1203Val
ENST00000578373.5:c.*3443A>T	ENSP00000463427.1:n.*3443A>T
ENST00000584450.5:c.*232A>T	ENSP00000463714.1:n.*232A>T
ENST00000584601.5:c.3563A>T	ENSP00000462438.1:p.Asp1188Val
NM_001005862.2:c.3563A>T , LRG_724t1:c.3563A>T	NP_001005862.1:p.Asp1188Val
NM_001289936.1:c.3608A>T , LRG_724t4:c.3608A>T	NP_001276865.1:p.Asp1203Val
NM_001289937.1:c.*232A>T	NP_001276866.1:n.*232A>T
NM_004448.3:c.3653A>T , LRG_724t2:c.3653A>T	NP_004439.2:p.Asp1218Val
NR_110535.1:n.3977A>T
XM_024450641.1:c.3791A>T	XP_024306409.1:p.Asp1264Val
XM_024450642.1:c.3746A>T	XP_024306410.1:p.Asp1249Val
XM_024450643.1:c.3701A>T	XP_024306411.1:p.Asp1234Val
NM_001005862.3:c.3563A>T	NP_001005862.1:p.Asp1188Val
NM_001289936.2:c.3608A>T	NP_001276865.1:p.Asp1203Val
NM_001289937.2:c.*232A>T	NP_001276866.1:n.*232A>T
NM_001382782.1:c.3563A>T	NP_001369711.1:p.Asp1188Val
NM_001382783.1:c.3563A>T	NP_001369712.1:p.Asp1188Val
NM_001382784.1:c.3770A>T	NP_001369713.1:p.Asp1257Val
NM_001382785.1:c.3755A>T	NP_001369714.1:p.Asp1252Val
NM_001382786.1:c.3734A>T	NP_001369715.1:p.Asp1245Val
NM_001382787.1:c.3728A>T	NP_001369716.1:p.Asp1243Val
NM_001382788.1:c.3683A>T	NP_001369717.1:p.Asp1228Val
NM_001382789.1:c.3674A>T	NP_001369718.1:p.Asp1225Val
NM_001382790.1:c.3650A>T	NP_001369719.1:p.Asp1217Val
NM_001382791.1:c.3644A>T	NP_001369720.1:p.Asp1215Val
NM_001382792.1:c.3617A>T	NP_001369721.1:p.Asp1206Val
NM_001382793.1:c.3611A>T	NP_001369722.1:p.Asp1204Val
NM_001382794.1:c.3611A>T	NP_001369723.1:p.Asp1204Val
NM_001382795.1:c.3605A>T	NP_001369724.1:p.Asp1202Val
NM_001382796.1:c.3566A>T	NP_001369725.1:p.Asp1189Val
NM_001382797.1:c.3554A>T	NP_001369726.1:p.Asp1185Val
NM_001382798.1:c.3497A>T	NP_001369727.1:p.Asp1166Val
NM_001382799.1:c.3473A>T	NP_001369728.1:p.Asp1158Val
NM_001382800.1:c.3467A>T	NP_001369729.1:p.Asp1156Val
NM_001382801.1:c.3449A>T	NP_001369730.1:p.Asp1150Val
NM_001382802.1:c.3395A>T	NP_001369731.1:p.Asp1132Val
NM_001382803.1:c.*232A>T	NP_001369732.1:n.*232A>T
NM_001382804.1:c.2825A>T	NP_001369733.1:p.Asp942Val
NM_001382805.1:c.2702A>T	NP_001369734.1:p.Asp901Val
NM_001382806.1:c.2615A>T	NP_001369735.1:p.Asp872Val
NM_004448.4:c.3653A>T MANE Select	NP_004439.2:p.Asp1218Val
NR_110535.2:n.3891A>T