Canonical Allele Identifier: CA2637636762
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727932del , CM000679.2:g.39727932del GRCh38
NC_000017.10:g.37884185del , CM000679.1:g.37884185del GRCh37
NC_000017.9:g.35137711del NCBI36
NG_007503.1:g.44793del , LRG_724:g.44793del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3656del MANE Select ENSP00000269571.4:p.Asn1219ThrfsTer?
ENST00000269571.9:c.3656del ENSP00000269571.4:p.Asn1219ThrfsTer?
ENST00000406381.6:c.3566del ENSP00000385185.2:p.Asn1189ThrfsTer?
ENST00000445658.6:c.2828del ENSP00000404047.2:p.Asn943ThrfsTer?
ENST00000541774.5:c.3611del ENSP00000446466.1:p.Asn1204ThrfsTer?
ENST00000578373.5:c.*3446del ENSP00000463427.1:n.*3446del
ENST00000584450.5:c.*235del ENSP00000463714.1:n.*235del
ENST00000584601.5:c.3566del ENSP00000462438.1:p.Asn1189ThrfsTer?
NM_001005862.2:c.3566del , LRG_724t1:c.3566del NP_001005862.1:p.Asn1189ThrfsTer?
NM_001289936.1:c.3611del , LRG_724t4:c.3611del NP_001276865.1:p.Asn1204ThrfsTer?
NM_001289937.1:c.*235del NP_001276866.1:n.*235del
NM_004448.3:c.3656del , LRG_724t2:c.3656del NP_004439.2:p.Asn1219ThrfsTer?
NR_110535.1:n.3980del
XM_024450641.1:c.3794del XP_024306409.1:p.Asn1265ThrfsTer?
XM_024450642.1:c.3749del XP_024306410.1:p.Asn1250ThrfsTer?
XM_024450643.1:c.3704del XP_024306411.1:p.Asn1235ThrfsTer?
NM_001005862.3:c.3566del NP_001005862.1:p.Asn1189ThrfsTer?
NM_001289936.2:c.3611del NP_001276865.1:p.Asn1204ThrfsTer?
NM_001289937.2:c.*235del NP_001276866.1:n.*235del
NM_001382782.1:c.3566del NP_001369711.1:p.Asn1189ThrfsTer?
NM_001382783.1:c.3566del NP_001369712.1:p.Asn1189ThrfsTer?
NM_001382784.1:c.3773del NP_001369713.1:p.Asn1258ThrfsTer?
NM_001382785.1:c.3758del NP_001369714.1:p.Asn1253ThrfsTer?
NM_001382786.1:c.3737del NP_001369715.1:p.Asn1246ThrfsTer?
NM_001382787.1:c.3731del NP_001369716.1:p.Asn1244ThrfsTer?
NM_001382788.1:c.3686del NP_001369717.1:p.Asn1229ThrfsTer?
NM_001382789.1:c.3677del NP_001369718.1:p.Asn1226ThrfsTer?
NM_001382790.1:c.3653del NP_001369719.1:p.Asn1218ThrfsTer?
NM_001382791.1:c.3647del NP_001369720.1:p.Asn1216ThrfsTer?
NM_001382792.1:c.3620del NP_001369721.1:p.Asn1207ThrfsTer?
NM_001382793.1:c.3614del NP_001369722.1:p.Asn1205ThrfsTer?
NM_001382794.1:c.3614del NP_001369723.1:p.Asn1205ThrfsTer?
NM_001382795.1:c.3608del NP_001369724.1:p.Asn1203ThrfsTer?
NM_001382796.1:c.3569del NP_001369725.1:p.Asn1190ThrfsTer?
NM_001382797.1:c.3557del NP_001369726.1:p.Asn1186ThrfsTer?
NM_001382798.1:c.3500del NP_001369727.1:p.Asn1167ThrfsTer?
NM_001382799.1:c.3476del NP_001369728.1:p.Asn1159ThrfsTer?
NM_001382800.1:c.3470del NP_001369729.1:p.Asn1157ThrfsTer?
NM_001382801.1:c.3452del NP_001369730.1:p.Asn1151ThrfsTer?
NM_001382802.1:c.3398del NP_001369731.1:p.Asn1133ThrfsTer?
NM_001382803.1:c.*235del NP_001369732.1:n.*235del
NM_001382804.1:c.2828del NP_001369733.1:p.Asn943ThrfsTer?
NM_001382805.1:c.2705del NP_001369734.1:p.Asn902ThrfsTer?
NM_001382806.1:c.2618del NP_001369735.1:p.Asn873ThrfsTer?
NM_004448.4:c.3656del MANE Select NP_004439.2:p.Asn1219ThrfsTer?
NR_110535.2:n.3894del