Canonical Allele Identifier: CA919838687

Gene: ERBB2

Linked Data

• dbSNP Id: rs1597886509

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724747del , CM000679.2:g.39724747del	GRCh38
NC_000017.10:g.37881000del , CM000679.1:g.37881000del	GRCh37
NC_000017.9:g.35134526del	NCBI36
NG_007503.1:g.41608del , LRG_724:g.41608del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2329del MANE Select	ENSP00000269571.4:p.Val777TrpfsTer14
ENST00000269571.9:c.2329del	ENSP00000269571.4:p.Val777TrpfsTer14
ENST00000406381.6:c.2239del	ENSP00000385185.2:p.Val747TrpfsTer14
ENST00000445658.6:c.1501del	ENSP00000404047.2:p.Val501TrpfsTer14
ENST00000541774.5:c.2284del	ENSP00000446466.1:p.Val762TrpfsTer14
ENST00000578373.5:c.*2119del	ENSP00000463427.1:n.*2119del
ENST00000580074.1:c.435del
ENST00000583038.5:n.3463del
ENST00000584450.5:c.2329del	ENSP00000463714.1:p.Val777TrpfsTer14
ENST00000584601.5:c.2239del	ENSP00000462438.1:p.Val747TrpfsTer14
NM_001005862.2:c.2239del , LRG_724t1:c.2239del	NP_001005862.1:p.Val747TrpfsTer14
NM_001289936.1:c.2284del , LRG_724t4:c.2284del	NP_001276865.1:p.Val762TrpfsTer14
NM_001289937.1:c.2329del	NP_001276866.1:p.Val777TrpfsTer14
NM_004448.3:c.2329del , LRG_724t2:c.2329del	NP_004439.2:p.Val777TrpfsTer14
NR_110535.1:n.2653del
XM_024450641.1:c.2467del	XP_024306409.1:p.Val823TrpfsTer14
XM_024450642.1:c.2422del	XP_024306410.1:p.Val808TrpfsTer14
XM_024450643.1:c.2377del	XP_024306411.1:p.Val793TrpfsTer14
NM_001005862.3:c.2239del	NP_001005862.1:p.Val747TrpfsTer14
NM_001289936.2:c.2284del	NP_001276865.1:p.Val762TrpfsTer14
NM_001289937.2:c.2329del	NP_001276866.1:p.Val777TrpfsTer14
NM_001382782.1:c.2239del	NP_001369711.1:p.Val747TrpfsTer14
NM_001382783.1:c.2239del	NP_001369712.1:p.Val747TrpfsTer14
NM_001382784.1:c.2446del	NP_001369713.1:p.Val816TrpfsTer14
NM_001382785.1:c.2431del	NP_001369714.1:p.Val811TrpfsTer14
NM_001382786.1:c.2410del	NP_001369715.1:p.Val804TrpfsTer14
NM_001382787.1:c.2404del	NP_001369716.1:p.Val802TrpfsTer14
NM_001382788.1:c.2359del	NP_001369717.1:p.Val787TrpfsTer14
NM_001382789.1:c.2350del	NP_001369718.1:p.Val784TrpfsTer14
NM_001382790.1:c.2326del	NP_001369719.1:p.Val776TrpfsTer14
NM_001382791.1:c.2320del	NP_001369720.1:p.Val774TrpfsTer14
NM_001382792.1:c.2293del	NP_001369721.1:p.Val765TrpfsTer14
NM_001382793.1:c.2287del	NP_001369722.1:p.Val763TrpfsTer14
NM_001382794.1:c.2287del	NP_001369723.1:p.Val763TrpfsTer14
NM_001382795.1:c.2281del	NP_001369724.1:p.Val761TrpfsTer14
NM_001382796.1:c.2329del	NP_001369725.1:p.Val777TrpfsTer14
NM_001382797.1:c.2230del	NP_001369726.1:p.Val744TrpfsTer14
NM_001382798.1:c.2329del	NP_001369727.1:p.Val777TrpfsTer14
NM_001382799.1:c.2149del	NP_001369728.1:p.Val717TrpfsTer14
NM_001382800.1:c.2308-302del	NP_001369729.1:n.2308-302del
NM_001382801.1:c.2281del	NP_001369730.1:p.Val761TrpfsTer14
NM_001382802.1:c.2071del	NP_001369731.1:p.Val691TrpfsTer14
NM_001382803.1:c.2287del	NP_001369732.1:p.Val763TrpfsTer14
NM_001382804.1:c.1501del	NP_001369733.1:p.Val501TrpfsTer14
NM_001382805.1:c.2208+1087del	NP_001369734.1:n.2208+1087del
NM_001382806.1:c.1291del	NP_001369735.1:p.Val431TrpfsTer14
NM_004448.4:c.2329del MANE Select	NP_004439.2:p.Val777TrpfsTer14
NR_110535.2:n.2567del