Canonical Allele Identifier: CA2637628543
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727415del , CM000679.2:g.39727415del GRCh38
NC_000017.10:g.37883668del , CM000679.1:g.37883668del GRCh37
NC_000017.9:g.35137194del NCBI36
NG_007503.1:g.44276del , LRG_724:g.44276del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3280del MANE Select ENSP00000269571.4:p.Ala1094GlnfsTer?
ENST00000269571.9:c.3280del ENSP00000269571.4:p.Ala1094GlnfsTer?
ENST00000406381.6:c.3190del ENSP00000385185.2:p.Ala1064GlnfsTer?
ENST00000445658.6:c.2452del ENSP00000404047.2:p.Ala818GlnfsTer?
ENST00000541774.5:c.3235del ENSP00000446466.1:p.Ala1079GlnfsTer?
ENST00000578373.5:c.*3070del ENSP00000463427.1:n.*3070del
ENST00000584450.5:c.3160-274del ENSP00000463714.1:n.3160-274del
ENST00000584601.5:c.3190del ENSP00000462438.1:p.Ala1064GlnfsTer?
NM_001005862.2:c.3190del , LRG_724t1:c.3190del NP_001005862.1:p.Ala1064GlnfsTer?
NM_001289936.1:c.3235del , LRG_724t4:c.3235del NP_001276865.1:p.Ala1079GlnfsTer?
NM_001289937.1:c.3160-274del NP_001276866.1:n.3160-274del
NM_004448.3:c.3280del , LRG_724t2:c.3280del NP_004439.2:p.Ala1094GlnfsTer?
NR_110535.1:n.3604del
XM_024450641.1:c.3418del XP_024306409.1:p.Ala1140GlnfsTer?
XM_024450642.1:c.3373del XP_024306410.1:p.Ala1125GlnfsTer?
XM_024450643.1:c.3328del XP_024306411.1:p.Ala1110GlnfsTer?
NM_001005862.3:c.3190del NP_001005862.1:p.Ala1064GlnfsTer?
NM_001289936.2:c.3235del NP_001276865.1:p.Ala1079GlnfsTer?
NM_001289937.2:c.3160-274del NP_001276866.1:n.3160-274del
NM_001382782.1:c.3190del NP_001369711.1:p.Ala1064GlnfsTer?
NM_001382783.1:c.3190del NP_001369712.1:p.Ala1064GlnfsTer?
NM_001382784.1:c.3397del NP_001369713.1:p.Ala1133GlnfsTer?
NM_001382785.1:c.3382del NP_001369714.1:p.Ala1128GlnfsTer?
NM_001382786.1:c.3361del NP_001369715.1:p.Ala1121GlnfsTer?
NM_001382787.1:c.3355del NP_001369716.1:p.Ala1119GlnfsTer?
NM_001382788.1:c.3310del NP_001369717.1:p.Ala1104GlnfsTer?
NM_001382789.1:c.3301del NP_001369718.1:p.Ala1101GlnfsTer?
NM_001382790.1:c.3277del NP_001369719.1:p.Ala1093GlnfsTer?
NM_001382791.1:c.3271del NP_001369720.1:p.Ala1091GlnfsTer?
NM_001382792.1:c.3244del NP_001369721.1:p.Ala1082GlnfsTer?
NM_001382793.1:c.3238del NP_001369722.1:p.Ala1080GlnfsTer?
NM_001382794.1:c.3238del NP_001369723.1:p.Ala1080GlnfsTer?
NM_001382795.1:c.3232del NP_001369724.1:p.Ala1078GlnfsTer?
NM_001382796.1:c.3193del NP_001369725.1:p.Ala1065GlnfsTer?
NM_001382797.1:c.3181del NP_001369726.1:p.Ala1061GlnfsTer?
NM_001382798.1:c.3124del NP_001369727.1:p.Ala1042GlnfsTer?
NM_001382799.1:c.3100del NP_001369728.1:p.Ala1034GlnfsTer?
NM_001382800.1:c.3094del NP_001369729.1:p.Ala1032GlnfsTer?
NM_001382801.1:c.3076del NP_001369730.1:p.Ala1026GlnfsTer?
NM_001382802.1:c.3022del NP_001369731.1:p.Ala1008GlnfsTer?
NM_001382803.1:c.3118-274del NP_001369732.1:n.3118-274del
NM_001382804.1:c.2452del NP_001369733.1:p.Ala818GlnfsTer?
NM_001382805.1:c.2329del NP_001369734.1:p.Ala777GlnfsTer?
NM_001382806.1:c.2242del NP_001369735.1:p.Ala748GlnfsTer?
NM_004448.4:c.3280del MANE Select NP_004439.2:p.Ala1094GlnfsTer?
NR_110535.2:n.3518del