Canonical Allele Identifier: CA499890659

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143295753
• MyVariant Identifiers: chr17:g.37884033A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727780A>G , CM000679.2:g.39727780A>G	GRCh38
NC_000017.10:g.37884033A>G , CM000679.1:g.37884033A>G	GRCh37
NC_000017.9:g.35137559A>G	NCBI36
NG_007503.1:g.44641A>G , LRG_724:g.44641A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3504A>G MANE Select	ENSP00000269571.4:p.Glu1168=
ENST00000269571.9:c.3504A>G	ENSP00000269571.4:p.Glu1168=
ENST00000406381.6:c.3414A>G	ENSP00000385185.2:p.Glu1138=
ENST00000445658.6:c.2676A>G	ENSP00000404047.2:p.Glu892=
ENST00000541774.5:c.3459A>G	ENSP00000446466.1:p.Glu1153=
ENST00000578373.5:c.*3294A>G	ENSP00000463427.1:n.*3294A>G
ENST00000584450.5:c.*83A>G	ENSP00000463714.1:n.*83A>G
ENST00000584601.5:c.3414A>G	ENSP00000462438.1:p.Glu1138=
NM_001005862.2:c.3414A>G , LRG_724t1:c.3414A>G	NP_001005862.1:p.Glu1138=
NM_001289936.1:c.3459A>G , LRG_724t4:c.3459A>G	NP_001276865.1:p.Glu1153=
NM_001289937.1:c.*83A>G	NP_001276866.1:n.*83A>G
NM_004448.3:c.3504A>G , LRG_724t2:c.3504A>G	NP_004439.2:p.Glu1168=
NR_110535.1:n.3828A>G
XM_024450641.1:c.3642A>G	XP_024306409.1:p.Glu1214=
XM_024450642.1:c.3597A>G	XP_024306410.1:p.Glu1199=
XM_024450643.1:c.3552A>G	XP_024306411.1:p.Glu1184=
NM_001005862.3:c.3414A>G	NP_001005862.1:p.Glu1138=
NM_001289936.2:c.3459A>G	NP_001276865.1:p.Glu1153=
NM_001289937.2:c.*83A>G	NP_001276866.1:n.*83A>G
NM_001382782.1:c.3414A>G	NP_001369711.1:p.Glu1138=
NM_001382783.1:c.3414A>G	NP_001369712.1:p.Glu1138=
NM_001382784.1:c.3621A>G	NP_001369713.1:p.Glu1207=
NM_001382785.1:c.3606A>G	NP_001369714.1:p.Glu1202=
NM_001382786.1:c.3585A>G	NP_001369715.1:p.Glu1195=
NM_001382787.1:c.3579A>G	NP_001369716.1:p.Glu1193=
NM_001382788.1:c.3534A>G	NP_001369717.1:p.Glu1178=
NM_001382789.1:c.3525A>G	NP_001369718.1:p.Glu1175=
NM_001382790.1:c.3501A>G	NP_001369719.1:p.Glu1167=
NM_001382791.1:c.3495A>G	NP_001369720.1:p.Glu1165=
NM_001382792.1:c.3468A>G	NP_001369721.1:p.Glu1156=
NM_001382793.1:c.3462A>G	NP_001369722.1:p.Glu1154=
NM_001382794.1:c.3462A>G	NP_001369723.1:p.Glu1154=
NM_001382795.1:c.3456A>G	NP_001369724.1:p.Glu1152=
NM_001382796.1:c.3417A>G	NP_001369725.1:p.Glu1139=
NM_001382797.1:c.3405A>G	NP_001369726.1:p.Glu1135=
NM_001382798.1:c.3348A>G	NP_001369727.1:p.Glu1116=
NM_001382799.1:c.3324A>G	NP_001369728.1:p.Glu1108=
NM_001382800.1:c.3318A>G	NP_001369729.1:p.Glu1106=
NM_001382801.1:c.3300A>G	NP_001369730.1:p.Glu1100=
NM_001382802.1:c.3246A>G	NP_001369731.1:p.Glu1082=
NM_001382803.1:c.*83A>G	NP_001369732.1:n.*83A>G
NM_001382804.1:c.2676A>G	NP_001369733.1:p.Glu892=
NM_001382805.1:c.2553A>G	NP_001369734.1:p.Glu851=
NM_001382806.1:c.2466A>G	NP_001369735.1:p.Glu822=
NM_004448.4:c.3504A>G MANE Select	NP_004439.2:p.Glu1168=
NR_110535.2:n.3742A>G