Canonical Allele Identifier: CA771855544

Gene: ERBB2

Linked Data

• dbSNP Id: rs1277581594
• MyVariant Identifiers: chr17:g.37880988_37880997del (hg19) ; chr17:g.39724735_39724744del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724738_39724747del , CM000679.2:g.39724738_39724747del	GRCh38
NC_000017.10:g.37880991_37881000del , CM000679.1:g.37880991_37881000del	GRCh37
NC_000017.9:g.35134517_35134526del	NCBI36
NG_007503.1:g.41599_41608del , LRG_724:g.41599_41608del

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2320_2329del MANE Select	ENSP00000269571.4:p.Met774TrpfsTer14
ENST00000269571.9:c.2320_2329del	ENSP00000269571.4:p.Met774TrpfsTer14
ENST00000406381.6:c.2230_2239del	ENSP00000385185.2:p.Met744TrpfsTer14
ENST00000445658.6:c.1492_1501del	ENSP00000404047.2:p.Met498TrpfsTer14
ENST00000541774.5:c.2275_2284del	ENSP00000446466.1:p.Met759TrpfsTer14
ENST00000578373.5:c.*2110_*2119del	ENSP00000463427.1:n.*2110_*2119del
ENST00000580074.1:c.426_435del
ENST00000583038.5:n.3454_3463del
ENST00000584450.5:c.2320_2329del	ENSP00000463714.1:p.Met774TrpfsTer14
ENST00000584601.5:c.2230_2239del	ENSP00000462438.1:p.Met744TrpfsTer14
NM_001005862.2:c.2230_2239del , LRG_724t1:c.2230_2239del	NP_001005862.1:p.Met744TrpfsTer14
NM_001289936.1:c.2275_2284del , LRG_724t4:c.2275_2284del	NP_001276865.1:p.Met759TrpfsTer14
NM_001289937.1:c.2320_2329del	NP_001276866.1:p.Met774TrpfsTer14
NM_004448.3:c.2320_2329del , LRG_724t2:c.2320_2329del	NP_004439.2:p.Met774TrpfsTer14
NR_110535.1:n.2644_2653del
XM_024450641.1:c.2458_2467del	XP_024306409.1:p.Met820TrpfsTer14
XM_024450642.1:c.2413_2422del	XP_024306410.1:p.Met805TrpfsTer14
XM_024450643.1:c.2368_2377del	XP_024306411.1:p.Met790TrpfsTer14
NM_001005862.3:c.2230_2239del	NP_001005862.1:p.Met744TrpfsTer14
NM_001289936.2:c.2275_2284del	NP_001276865.1:p.Met759TrpfsTer14
NM_001289937.2:c.2320_2329del	NP_001276866.1:p.Met774TrpfsTer14
NM_001382782.1:c.2230_2239del	NP_001369711.1:p.Met744TrpfsTer14
NM_001382783.1:c.2230_2239del	NP_001369712.1:p.Met744TrpfsTer14
NM_001382784.1:c.2437_2446del	NP_001369713.1:p.Met813TrpfsTer14
NM_001382785.1:c.2422_2431del	NP_001369714.1:p.Met808TrpfsTer14
NM_001382786.1:c.2401_2410del	NP_001369715.1:p.Met801TrpfsTer14
NM_001382787.1:c.2395_2404del	NP_001369716.1:p.Met799TrpfsTer14
NM_001382788.1:c.2350_2359del	NP_001369717.1:p.Met784TrpfsTer14
NM_001382789.1:c.2341_2350del	NP_001369718.1:p.Met781TrpfsTer14
NM_001382790.1:c.2317_2326del	NP_001369719.1:p.Met773TrpfsTer14
NM_001382791.1:c.2311_2320del	NP_001369720.1:p.Met771TrpfsTer14
NM_001382792.1:c.2284_2293del	NP_001369721.1:p.Met762TrpfsTer14
NM_001382793.1:c.2278_2287del	NP_001369722.1:p.Met760TrpfsTer14
NM_001382794.1:c.2278_2287del	NP_001369723.1:p.Met760TrpfsTer14
NM_001382795.1:c.2272_2281del	NP_001369724.1:p.Met758TrpfsTer14
NM_001382796.1:c.2320_2329del	NP_001369725.1:p.Met774TrpfsTer14
NM_001382797.1:c.2221_2230del	NP_001369726.1:p.Met741TrpfsTer14
NM_001382798.1:c.2320_2329del	NP_001369727.1:p.Met774TrpfsTer14
NM_001382799.1:c.2140_2149del	NP_001369728.1:p.Met714TrpfsTer14
NM_001382800.1:c.2308-311_2308-302del	NP_001369729.1:n.2308-311_2308-302del
NM_001382801.1:c.2272_2281del	NP_001369730.1:p.Met758TrpfsTer14
NM_001382802.1:c.2062_2071del	NP_001369731.1:p.Met688TrpfsTer14
NM_001382803.1:c.2278_2287del	NP_001369732.1:p.Met760TrpfsTer14
NM_001382804.1:c.1492_1501del	NP_001369733.1:p.Met498TrpfsTer14
NM_001382805.1:c.2208+1078_2208+1087del	NP_001369734.1:n.2208+1078_2208+1087del
NM_001382806.1:c.1282_1291del	NP_001369735.1:p.Met428TrpfsTer14
NM_004448.4:c.2320_2329del MANE Select	NP_004439.2:p.Met774TrpfsTer14
NR_110535.2:n.2558_2567del