Canonical Allele Identifier: CA2733496999
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2143234420

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727325del , CM000679.2:g.39727325del GRCh38
NC_000017.10:g.37883578del , CM000679.1:g.37883578del GRCh37
NC_000017.9:g.35137104del NCBI36
NG_007503.1:g.44186del , LRG_724:g.44186del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3190del MANE Select ENSP00000269571.4:p.Glu1064SerfsTer?
ENST00000269571.9:c.3190del ENSP00000269571.4:p.Glu1064SerfsTer?
ENST00000406381.6:c.3100del ENSP00000385185.2:p.Glu1034SerfsTer?
ENST00000445658.6:c.2362del ENSP00000404047.2:p.Glu788SerfsTer?
ENST00000541774.5:c.3145del ENSP00000446466.1:p.Glu1049SerfsTer?
ENST00000578373.5:c.*2980del ENSP00000463427.1:n.*2980del
ENST00000584450.5:c.3159+322del ENSP00000463714.1:n.3159+322del
ENST00000584601.5:c.3100del ENSP00000462438.1:p.Glu1034SerfsTer?
NM_001005862.2:c.3100del , LRG_724t1:c.3100del NP_001005862.1:p.Glu1034SerfsTer?
NM_001289936.1:c.3145del , LRG_724t4:c.3145del NP_001276865.1:p.Glu1049SerfsTer?
NM_001289937.1:c.3159+322del NP_001276866.1:n.3159+322del
NM_004448.3:c.3190del , LRG_724t2:c.3190del NP_004439.2:p.Glu1064SerfsTer?
NR_110535.1:n.3514del
XM_024450641.1:c.3328del XP_024306409.1:p.Glu1110SerfsTer?
XM_024450642.1:c.3283del XP_024306410.1:p.Glu1095SerfsTer?
XM_024450643.1:c.3238del XP_024306411.1:p.Glu1080SerfsTer?
NM_001005862.3:c.3100del NP_001005862.1:p.Glu1034SerfsTer?
NM_001289936.2:c.3145del NP_001276865.1:p.Glu1049SerfsTer?
NM_001289937.2:c.3159+322del NP_001276866.1:n.3159+322del
NM_001382782.1:c.3100del NP_001369711.1:p.Glu1034SerfsTer?
NM_001382783.1:c.3100del NP_001369712.1:p.Glu1034SerfsTer?
NM_001382784.1:c.3307del NP_001369713.1:p.Glu1103SerfsTer?
NM_001382785.1:c.3292del NP_001369714.1:p.Glu1098SerfsTer?
NM_001382786.1:c.3271del NP_001369715.1:p.Glu1091SerfsTer?
NM_001382787.1:c.3265del NP_001369716.1:p.Glu1089SerfsTer?
NM_001382788.1:c.3220del NP_001369717.1:p.Glu1074SerfsTer?
NM_001382789.1:c.3211del NP_001369718.1:p.Glu1071SerfsTer?
NM_001382790.1:c.3187del NP_001369719.1:p.Glu1063SerfsTer?
NM_001382791.1:c.3181del NP_001369720.1:p.Glu1061SerfsTer?
NM_001382792.1:c.3154del NP_001369721.1:p.Glu1052SerfsTer?
NM_001382793.1:c.3148del NP_001369722.1:p.Glu1050SerfsTer?
NM_001382794.1:c.3148del NP_001369723.1:p.Glu1050SerfsTer?
NM_001382795.1:c.3142del NP_001369724.1:p.Glu1048SerfsTer?
NM_001382796.1:c.3103del NP_001369725.1:p.Glu1035SerfsTer?
NM_001382797.1:c.3091del NP_001369726.1:p.Glu1031SerfsTer?
NM_001382798.1:c.3034del NP_001369727.1:p.Glu1012SerfsTer?
NM_001382799.1:c.3010del NP_001369728.1:p.Glu1004SerfsTer?
NM_001382800.1:c.3004del NP_001369729.1:p.Glu1002SerfsTer?
NM_001382801.1:c.2986del NP_001369730.1:p.Glu996SerfsTer?
NM_001382802.1:c.2932del NP_001369731.1:p.Glu978SerfsTer?
NM_001382803.1:c.3117+322del NP_001369732.1:n.3117+322del
NM_001382804.1:c.2362del NP_001369733.1:p.Glu788SerfsTer?
NM_001382805.1:c.2239del NP_001369734.1:p.Glu747SerfsTer?
NM_001382806.1:c.2152del NP_001369735.1:p.Glu718SerfsTer?
NM_004448.4:c.3190del MANE Select NP_004439.2:p.Glu1064SerfsTer?
NR_110535.2:n.3428del