Canonical Allele Identifier: CA2637630980
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727920del , CM000679.2:g.39727920del GRCh38
NC_000017.10:g.37884173del , CM000679.1:g.37884173del GRCh37
NC_000017.9:g.35137699del NCBI36
NG_007503.1:g.44781del , LRG_724:g.44781del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3644del MANE Select ENSP00000269571.4:p.Pro1215GlnfsTer?
ENST00000269571.9:c.3644del ENSP00000269571.4:p.Pro1215GlnfsTer?
ENST00000406381.6:c.3554del ENSP00000385185.2:p.Pro1185GlnfsTer?
ENST00000445658.6:c.2816del ENSP00000404047.2:p.Pro939GlnfsTer?
ENST00000541774.5:c.3599del ENSP00000446466.1:p.Pro1200GlnfsTer?
ENST00000578373.5:c.*3434del ENSP00000463427.1:n.*3434del
ENST00000584450.5:c.*223del ENSP00000463714.1:n.*223del
ENST00000584601.5:c.3554del ENSP00000462438.1:p.Pro1185GlnfsTer?
NM_001005862.2:c.3554del , LRG_724t1:c.3554del NP_001005862.1:p.Pro1185GlnfsTer?
NM_001289936.1:c.3599del , LRG_724t4:c.3599del NP_001276865.1:p.Pro1200GlnfsTer?
NM_001289937.1:c.*223del NP_001276866.1:n.*223del
NM_004448.3:c.3644del , LRG_724t2:c.3644del NP_004439.2:p.Pro1215GlnfsTer?
NR_110535.1:n.3968del
XM_024450641.1:c.3782del XP_024306409.1:p.Pro1261GlnfsTer?
XM_024450642.1:c.3737del XP_024306410.1:p.Pro1246GlnfsTer?
XM_024450643.1:c.3692del XP_024306411.1:p.Pro1231GlnfsTer?
NM_001005862.3:c.3554del NP_001005862.1:p.Pro1185GlnfsTer?
NM_001289936.2:c.3599del NP_001276865.1:p.Pro1200GlnfsTer?
NM_001289937.2:c.*223del NP_001276866.1:n.*223del
NM_001382782.1:c.3554del NP_001369711.1:p.Pro1185GlnfsTer?
NM_001382783.1:c.3554del NP_001369712.1:p.Pro1185GlnfsTer?
NM_001382784.1:c.3761del NP_001369713.1:p.Pro1254GlnfsTer?
NM_001382785.1:c.3746del NP_001369714.1:p.Pro1249GlnfsTer?
NM_001382786.1:c.3725del NP_001369715.1:p.Pro1242GlnfsTer?
NM_001382787.1:c.3719del NP_001369716.1:p.Pro1240GlnfsTer?
NM_001382788.1:c.3674del NP_001369717.1:p.Pro1225GlnfsTer?
NM_001382789.1:c.3665del NP_001369718.1:p.Pro1222GlnfsTer?
NM_001382790.1:c.3641del NP_001369719.1:p.Pro1214GlnfsTer?
NM_001382791.1:c.3635del NP_001369720.1:p.Pro1212GlnfsTer?
NM_001382792.1:c.3608del NP_001369721.1:p.Pro1203GlnfsTer?
NM_001382793.1:c.3602del NP_001369722.1:p.Pro1201GlnfsTer?
NM_001382794.1:c.3602del NP_001369723.1:p.Pro1201GlnfsTer?
NM_001382795.1:c.3596del NP_001369724.1:p.Pro1199GlnfsTer?
NM_001382796.1:c.3557del NP_001369725.1:p.Pro1186GlnfsTer?
NM_001382797.1:c.3545del NP_001369726.1:p.Pro1182GlnfsTer?
NM_001382798.1:c.3488del NP_001369727.1:p.Pro1163GlnfsTer?
NM_001382799.1:c.3464del NP_001369728.1:p.Pro1155GlnfsTer?
NM_001382800.1:c.3458del NP_001369729.1:p.Pro1153GlnfsTer?
NM_001382801.1:c.3440del NP_001369730.1:p.Pro1147GlnfsTer?
NM_001382802.1:c.3386del NP_001369731.1:p.Pro1129GlnfsTer?
NM_001382803.1:c.*223del NP_001369732.1:n.*223del
NM_001382804.1:c.2816del NP_001369733.1:p.Pro939GlnfsTer?
NM_001382805.1:c.2693del NP_001369734.1:p.Pro898GlnfsTer?
NM_001382806.1:c.2606del NP_001369735.1:p.Pro869GlnfsTer?
NM_004448.4:c.3644del MANE Select NP_004439.2:p.Pro1215GlnfsTer?
NR_110535.2:n.3882del