Canonical Allele Identifier: CA499890730

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143301443
• MyVariant Identifiers: chr17:g.37884081T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727828T>A , CM000679.2:g.39727828T>A	GRCh38
NC_000017.10:g.37884081T>A , CM000679.1:g.37884081T>A	GRCh37
NC_000017.9:g.35137607T>A	NCBI36
NG_007503.1:g.44689T>A , LRG_724:g.44689T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3552T>A MANE Select	ENSP00000269571.4:p.Val1184=
ENST00000269571.9:c.3552T>A	ENSP00000269571.4:p.Val1184=
ENST00000406381.6:c.3462T>A	ENSP00000385185.2:p.Val1154=
ENST00000445658.6:c.2724T>A	ENSP00000404047.2:p.Val908=
ENST00000541774.5:c.3507T>A	ENSP00000446466.1:p.Val1169=
ENST00000578373.5:c.*3342T>A	ENSP00000463427.1:n.*3342T>A
ENST00000584450.5:c.*131T>A	ENSP00000463714.1:n.*131T>A
ENST00000584601.5:c.3462T>A	ENSP00000462438.1:p.Val1154=
NM_001005862.2:c.3462T>A , LRG_724t1:c.3462T>A	NP_001005862.1:p.Val1154=
NM_001289936.1:c.3507T>A , LRG_724t4:c.3507T>A	NP_001276865.1:p.Val1169=
NM_001289937.1:c.*131T>A	NP_001276866.1:n.*131T>A
NM_004448.3:c.3552T>A , LRG_724t2:c.3552T>A	NP_004439.2:p.Val1184=
NR_110535.1:n.3876T>A
XM_024450641.1:c.3690T>A	XP_024306409.1:p.Val1230=
XM_024450642.1:c.3645T>A	XP_024306410.1:p.Val1215=
XM_024450643.1:c.3600T>A	XP_024306411.1:p.Val1200=
NM_001005862.3:c.3462T>A	NP_001005862.1:p.Val1154=
NM_001289936.2:c.3507T>A	NP_001276865.1:p.Val1169=
NM_001289937.2:c.*131T>A	NP_001276866.1:n.*131T>A
NM_001382782.1:c.3462T>A	NP_001369711.1:p.Val1154=
NM_001382783.1:c.3462T>A	NP_001369712.1:p.Val1154=
NM_001382784.1:c.3669T>A	NP_001369713.1:p.Val1223=
NM_001382785.1:c.3654T>A	NP_001369714.1:p.Val1218=
NM_001382786.1:c.3633T>A	NP_001369715.1:p.Val1211=
NM_001382787.1:c.3627T>A	NP_001369716.1:p.Val1209=
NM_001382788.1:c.3582T>A	NP_001369717.1:p.Val1194=
NM_001382789.1:c.3573T>A	NP_001369718.1:p.Val1191=
NM_001382790.1:c.3549T>A	NP_001369719.1:p.Val1183=
NM_001382791.1:c.3543T>A	NP_001369720.1:p.Val1181=
NM_001382792.1:c.3516T>A	NP_001369721.1:p.Val1172=
NM_001382793.1:c.3510T>A	NP_001369722.1:p.Val1170=
NM_001382794.1:c.3510T>A	NP_001369723.1:p.Val1170=
NM_001382795.1:c.3504T>A	NP_001369724.1:p.Val1168=
NM_001382796.1:c.3465T>A	NP_001369725.1:p.Val1155=
NM_001382797.1:c.3453T>A	NP_001369726.1:p.Val1151=
NM_001382798.1:c.3396T>A	NP_001369727.1:p.Val1132=
NM_001382799.1:c.3372T>A	NP_001369728.1:p.Val1124=
NM_001382800.1:c.3366T>A	NP_001369729.1:p.Val1122=
NM_001382801.1:c.3348T>A	NP_001369730.1:p.Val1116=
NM_001382802.1:c.3294T>A	NP_001369731.1:p.Val1098=
NM_001382803.1:c.*131T>A	NP_001369732.1:n.*131T>A
NM_001382804.1:c.2724T>A	NP_001369733.1:p.Val908=
NM_001382805.1:c.2601T>A	NP_001369734.1:p.Val867=
NM_001382806.1:c.2514T>A	NP_001369735.1:p.Val838=
NM_004448.4:c.3552T>A MANE Select	NP_004439.2:p.Val1184=
NR_110535.2:n.3790T>A