Canonical Allele Identifier: CA399314476

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884205G>T (hg19) ; chr17:g.39727952G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727952G>T , CM000679.2:g.39727952G>T	GRCh38
NC_000017.10:g.37884205G>T , CM000679.1:g.37884205G>T	GRCh37
NC_000017.9:g.35137731G>T	NCBI36
NG_007503.1:g.44813G>T , LRG_724:g.44813G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3676G>T MANE Select	ENSP00000269571.4:p.Asp1226Tyr
ENST00000269571.9:c.3676G>T	ENSP00000269571.4:p.Asp1226Tyr
ENST00000406381.6:c.3586G>T	ENSP00000385185.2:p.Asp1196Tyr
ENST00000445658.6:c.2848G>T	ENSP00000404047.2:p.Asp950Tyr
ENST00000541774.5:c.3631G>T	ENSP00000446466.1:p.Asp1211Tyr
ENST00000578373.5:c.*3466G>T	ENSP00000463427.1:n.*3466G>T
ENST00000584450.5:c.*255G>T	ENSP00000463714.1:n.*255G>T
ENST00000584601.5:c.3586G>T	ENSP00000462438.1:p.Asp1196Tyr
NM_001005862.2:c.3586G>T , LRG_724t1:c.3586G>T	NP_001005862.1:p.Asp1196Tyr
NM_001289936.1:c.3631G>T , LRG_724t4:c.3631G>T	NP_001276865.1:p.Asp1211Tyr
NM_001289937.1:c.*255G>T	NP_001276866.1:n.*255G>T
NM_004448.3:c.3676G>T , LRG_724t2:c.3676G>T	NP_004439.2:p.Asp1226Tyr
NR_110535.1:n.4000G>T
XM_024450641.1:c.3814G>T	XP_024306409.1:p.Asp1272Tyr
XM_024450642.1:c.3769G>T	XP_024306410.1:p.Asp1257Tyr
XM_024450643.1:c.3724G>T	XP_024306411.1:p.Asp1242Tyr
NM_001005862.3:c.3586G>T	NP_001005862.1:p.Asp1196Tyr
NM_001289936.2:c.3631G>T	NP_001276865.1:p.Asp1211Tyr
NM_001289937.2:c.*255G>T	NP_001276866.1:n.*255G>T
NM_001382782.1:c.3586G>T	NP_001369711.1:p.Asp1196Tyr
NM_001382783.1:c.3586G>T	NP_001369712.1:p.Asp1196Tyr
NM_001382784.1:c.3793G>T	NP_001369713.1:p.Asp1265Tyr
NM_001382785.1:c.3778G>T	NP_001369714.1:p.Asp1260Tyr
NM_001382786.1:c.3757G>T	NP_001369715.1:p.Asp1253Tyr
NM_001382787.1:c.3751G>T	NP_001369716.1:p.Asp1251Tyr
NM_001382788.1:c.3706G>T	NP_001369717.1:p.Asp1236Tyr
NM_001382789.1:c.3697G>T	NP_001369718.1:p.Asp1233Tyr
NM_001382790.1:c.3673G>T	NP_001369719.1:p.Asp1225Tyr
NM_001382791.1:c.3667G>T	NP_001369720.1:p.Asp1223Tyr
NM_001382792.1:c.3640G>T	NP_001369721.1:p.Asp1214Tyr
NM_001382793.1:c.3634G>T	NP_001369722.1:p.Asp1212Tyr
NM_001382794.1:c.3634G>T	NP_001369723.1:p.Asp1212Tyr
NM_001382795.1:c.3628G>T	NP_001369724.1:p.Asp1210Tyr
NM_001382796.1:c.3589G>T	NP_001369725.1:p.Asp1197Tyr
NM_001382797.1:c.3577G>T	NP_001369726.1:p.Asp1193Tyr
NM_001382798.1:c.3520G>T	NP_001369727.1:p.Asp1174Tyr
NM_001382799.1:c.3496G>T	NP_001369728.1:p.Asp1166Tyr
NM_001382800.1:c.3490G>T	NP_001369729.1:p.Asp1164Tyr
NM_001382801.1:c.3472G>T	NP_001369730.1:p.Asp1158Tyr
NM_001382802.1:c.3418G>T	NP_001369731.1:p.Asp1140Tyr
NM_001382803.1:c.*255G>T	NP_001369732.1:n.*255G>T
NM_001382804.1:c.2848G>T	NP_001369733.1:p.Asp950Tyr
NM_001382805.1:c.2725G>T	NP_001369734.1:p.Asp909Tyr
NM_001382806.1:c.2638G>T	NP_001369735.1:p.Asp880Tyr
NM_004448.4:c.3676G>T MANE Select	NP_004439.2:p.Asp1226Tyr
NR_110535.2:n.3914G>T