Canonical Allele Identifier: CA891842275
Community Standard Title: NM_004448.4(ERBB2):c.2262_2276del (p.Leu755_Thr759del)
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39723965_39723979del , CM000679.2:g.39723965_39723979del GRCh38
NC_000017.10:g.37880218_37880232del , CM000679.1:g.37880218_37880232del GRCh37
NC_000017.9:g.35133744_35133758del NCBI36
NG_007503.1:g.40826_40840del , LRG_724:g.40826_40840del

Transcript Alleles

HGVS Amino-acid Change
NM_004448.4:c.2262_2276del MANE Select NP_004439.2:p.Leu755_Thr759del
ENST00000269571.10:c.2262_2276del MANE Select ENSP00000269571.4:p.Leu755_Thr759del
NM_001005862.2:c.2172_2186del , LRG_724t1:c.2172_2186del NP_001005862.1:p.Leu725_Thr729del
NM_001005862.3:c.2172_2186del NP_001005862.1:p.Leu725_Thr729del
NM_001289936.1:c.2217_2231del , LRG_724t4:c.2217_2231del NP_001276865.1:p.Leu740_Thr744del
NM_001289936.2:c.2217_2231del NP_001276865.1:p.Leu740_Thr744del
NM_001289937.1:c.2262_2276del NP_001276866.1:p.Leu755_Thr759del
NM_001289937.2:c.2262_2276del NP_001276866.1:p.Leu755_Thr759del
NM_001382782.1:c.2172_2186del NP_001369711.1:p.Leu725_Thr729del
NM_001382783.1:c.2172_2186del NP_001369712.1:p.Leu725_Thr729del
NM_001382784.1:c.2379_2393del NP_001369713.1:p.Leu794_Thr798del
NM_001382785.1:c.2364_2378del NP_001369714.1:p.Leu789_Thr793del
NM_001382786.1:c.2343_2357del NP_001369715.1:p.Leu782_Thr786del
NM_001382787.1:c.2337_2351del NP_001369716.1:p.Leu780_Thr784del
NM_001382788.1:c.2292_2306del NP_001369717.1:p.Leu765_Thr769del
NM_001382789.1:c.2283_2297del NP_001369718.1:p.Leu762_Thr766del
NM_001382790.1:c.2259_2273del NP_001369719.1:p.Leu754_Thr758del
NM_001382791.1:c.2253_2267del NP_001369720.1:p.Leu752_Thr756del
NM_001382792.1:c.2226_2240del NP_001369721.1:p.Leu743_Thr747del
NM_001382793.1:c.2220_2234del NP_001369722.1:p.Leu741_Thr745del
NM_001382794.1:c.2220_2234del NP_001369723.1:p.Leu741_Thr745del
NM_001382795.1:c.2214_2228del NP_001369724.1:p.Leu739_Thr743del
NM_001382796.1:c.2262_2276del NP_001369725.1:p.Leu755_Thr759del
NM_001382797.1:c.2208+305_2208+319del NP_001369726.1:n.2208+305_2208+319del
NM_001382798.1:c.2262_2276del NP_001369727.1:p.Leu755_Thr759del
NM_001382799.1:c.2082_2096del NP_001369728.1:p.Leu695_Thr699del
NM_001382800.1:c.2262_2276del NP_001369729.1:p.Leu755_Thr759del
NM_001382801.1:c.2214_2228del NP_001369730.1:p.Leu739_Thr743del
NM_001382802.1:c.2004_2018del NP_001369731.1:p.Leu669_Thr673del
NM_001382803.1:c.2220_2234del NP_001369732.1:p.Leu741_Thr745del
NM_001382804.1:c.1434_1448del NP_001369733.1:p.Leu479_Thr483del
NM_001382805.1:c.2208+305_2208+319del NP_001369734.1:n.2208+305_2208+319del
NM_001382806.1:c.1224_1238del NP_001369735.1:p.Leu409_Thr413del
NM_004448.3:c.2262_2276del , LRG_724t2:c.2262_2276del NP_004439.2:p.Leu755_Thr759del
NR_110535.1:n.2586_2600del
NR_110535.2:n.2500_2514del
ENST00000269571.9:c.2262_2276del ENSP00000269571.4:p.Leu755_Thr759del
ENST00000406381.6:c.2172_2186del ENSP00000385185.2:p.Leu725_Thr729del
ENST00000445658.6:c.1434_1448del ENSP00000404047.2:p.Leu479_Thr483del
ENST00000541774.5:c.2217_2231del ENSP00000446466.1:p.Leu740_Thr744del
ENST00000578373.5:c.*2052_*2066del ENSP00000463427.1:n.*2052_*2066del
ENST00000580074.1:c.368_382del
ENST00000583038.5:n.3396_3410del
ENST00000584450.5:c.2262_2276del ENSP00000463714.1:p.Leu755_Thr759del
ENST00000584601.5:c.2172_2186del ENSP00000462438.1:p.Leu725_Thr729del
XM_024450641.1:c.2400_2414del XP_024306409.1:p.Leu801_Thr805del
XM_024450642.1:c.2355_2369del XP_024306410.1:p.Leu786_Thr790del
XM_024450643.1:c.2310_2324del XP_024306411.1:p.Leu771_Thr775del