Canonical Allele Identifier: CA399313494

Gene: ERBB2

Linked Data

• dbSNP Id: rs767230649
• MyVariant Identifiers: chr17:g.37884078C>A (hg19) ; chr17:g.39727825C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727825C>A , CM000679.2:g.39727825C>A	GRCh38
NC_000017.10:g.37884078C>A , CM000679.1:g.37884078C>A	GRCh37
NC_000017.9:g.35137604C>A	NCBI36
NG_007503.1:g.44686C>A , LRG_724:g.44686C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3549C>A MANE Select	ENSP00000269571.4:p.Asp1183Glu
ENST00000269571.9:c.3549C>A	ENSP00000269571.4:p.Asp1183Glu
ENST00000406381.6:c.3459C>A	ENSP00000385185.2:p.Asp1153Glu
ENST00000445658.6:c.2721C>A	ENSP00000404047.2:p.Asp907Glu
ENST00000541774.5:c.3504C>A	ENSP00000446466.1:p.Asp1168Glu
ENST00000578373.5:c.*3339C>A	ENSP00000463427.1:n.*3339C>A
ENST00000584450.5:c.*128C>A	ENSP00000463714.1:n.*128C>A
ENST00000584601.5:c.3459C>A	ENSP00000462438.1:p.Asp1153Glu
NM_001005862.2:c.3459C>A , LRG_724t1:c.3459C>A	NP_001005862.1:p.Asp1153Glu
NM_001289936.1:c.3504C>A , LRG_724t4:c.3504C>A	NP_001276865.1:p.Asp1168Glu
NM_001289937.1:c.*128C>A	NP_001276866.1:n.*128C>A
NM_004448.3:c.3549C>A , LRG_724t2:c.3549C>A	NP_004439.2:p.Asp1183Glu
NR_110535.1:n.3873C>A
XM_024450641.1:c.3687C>A	XP_024306409.1:p.Asp1229Glu
XM_024450642.1:c.3642C>A	XP_024306410.1:p.Asp1214Glu
XM_024450643.1:c.3597C>A	XP_024306411.1:p.Asp1199Glu
NM_001005862.3:c.3459C>A	NP_001005862.1:p.Asp1153Glu
NM_001289936.2:c.3504C>A	NP_001276865.1:p.Asp1168Glu
NM_001289937.2:c.*128C>A	NP_001276866.1:n.*128C>A
NM_001382782.1:c.3459C>A	NP_001369711.1:p.Asp1153Glu
NM_001382783.1:c.3459C>A	NP_001369712.1:p.Asp1153Glu
NM_001382784.1:c.3666C>A	NP_001369713.1:p.Asp1222Glu
NM_001382785.1:c.3651C>A	NP_001369714.1:p.Asp1217Glu
NM_001382786.1:c.3630C>A	NP_001369715.1:p.Asp1210Glu
NM_001382787.1:c.3624C>A	NP_001369716.1:p.Asp1208Glu
NM_001382788.1:c.3579C>A	NP_001369717.1:p.Asp1193Glu
NM_001382789.1:c.3570C>A	NP_001369718.1:p.Asp1190Glu
NM_001382790.1:c.3546C>A	NP_001369719.1:p.Asp1182Glu
NM_001382791.1:c.3540C>A	NP_001369720.1:p.Asp1180Glu
NM_001382792.1:c.3513C>A	NP_001369721.1:p.Asp1171Glu
NM_001382793.1:c.3507C>A	NP_001369722.1:p.Asp1169Glu
NM_001382794.1:c.3507C>A	NP_001369723.1:p.Asp1169Glu
NM_001382795.1:c.3501C>A	NP_001369724.1:p.Asp1167Glu
NM_001382796.1:c.3462C>A	NP_001369725.1:p.Asp1154Glu
NM_001382797.1:c.3450C>A	NP_001369726.1:p.Asp1150Glu
NM_001382798.1:c.3393C>A	NP_001369727.1:p.Asp1131Glu
NM_001382799.1:c.3369C>A	NP_001369728.1:p.Asp1123Glu
NM_001382800.1:c.3363C>A	NP_001369729.1:p.Asp1121Glu
NM_001382801.1:c.3345C>A	NP_001369730.1:p.Asp1115Glu
NM_001382802.1:c.3291C>A	NP_001369731.1:p.Asp1097Glu
NM_001382803.1:c.*128C>A	NP_001369732.1:n.*128C>A
NM_001382804.1:c.2721C>A	NP_001369733.1:p.Asp907Glu
NM_001382805.1:c.2598C>A	NP_001369734.1:p.Asp866Glu
NM_001382806.1:c.2511C>A	NP_001369735.1:p.Asp837Glu
NM_004448.4:c.3549C>A MANE Select	NP_004439.2:p.Asp1183Glu
NR_110535.2:n.3787C>A