Canonical Allele Identifier: CA399314171
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727915C>G , CM000679.2:g.39727915C>G GRCh38
NC_000017.10:g.37884168C>G , CM000679.1:g.37884168C>G GRCh37
NC_000017.9:g.35137694C>G NCBI36
NG_007503.1:g.44776C>G , LRG_724:g.44776C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3639C>G MANE Select ENSP00000269571.4:p.Phe1213Leu
ENST00000269571.9:c.3639C>G ENSP00000269571.4:p.Phe1213Leu
ENST00000406381.6:c.3549C>G ENSP00000385185.2:p.Phe1183Leu
ENST00000445658.6:c.2811C>G ENSP00000404047.2:p.Phe937Leu
ENST00000541774.5:c.3594C>G ENSP00000446466.1:p.Phe1198Leu
ENST00000578373.5:c.*3429C>G ENSP00000463427.1:n.*3429C>G
ENST00000584450.5:c.*218C>G ENSP00000463714.1:n.*218C>G
ENST00000584601.5:c.3549C>G ENSP00000462438.1:p.Phe1183Leu
NM_001005862.2:c.3549C>G , LRG_724t1:c.3549C>G NP_001005862.1:p.Phe1183Leu
NM_001289936.1:c.3594C>G , LRG_724t4:c.3594C>G NP_001276865.1:p.Phe1198Leu
NM_001289937.1:c.*218C>G NP_001276866.1:n.*218C>G
NM_004448.3:c.3639C>G , LRG_724t2:c.3639C>G NP_004439.2:p.Phe1213Leu
NR_110535.1:n.3963C>G
XM_024450641.1:c.3777C>G XP_024306409.1:p.Phe1259Leu
XM_024450642.1:c.3732C>G XP_024306410.1:p.Phe1244Leu
XM_024450643.1:c.3687C>G XP_024306411.1:p.Phe1229Leu
NM_001005862.3:c.3549C>G NP_001005862.1:p.Phe1183Leu
NM_001289936.2:c.3594C>G NP_001276865.1:p.Phe1198Leu
NM_001289937.2:c.*218C>G NP_001276866.1:n.*218C>G
NM_001382782.1:c.3549C>G NP_001369711.1:p.Phe1183Leu
NM_001382783.1:c.3549C>G NP_001369712.1:p.Phe1183Leu
NM_001382784.1:c.3756C>G NP_001369713.1:p.Phe1252Leu
NM_001382785.1:c.3741C>G NP_001369714.1:p.Phe1247Leu
NM_001382786.1:c.3720C>G NP_001369715.1:p.Phe1240Leu
NM_001382787.1:c.3714C>G NP_001369716.1:p.Phe1238Leu
NM_001382788.1:c.3669C>G NP_001369717.1:p.Phe1223Leu
NM_001382789.1:c.3660C>G NP_001369718.1:p.Phe1220Leu
NM_001382790.1:c.3636C>G NP_001369719.1:p.Phe1212Leu
NM_001382791.1:c.3630C>G NP_001369720.1:p.Phe1210Leu
NM_001382792.1:c.3603C>G NP_001369721.1:p.Phe1201Leu
NM_001382793.1:c.3597C>G NP_001369722.1:p.Phe1199Leu
NM_001382794.1:c.3597C>G NP_001369723.1:p.Phe1199Leu
NM_001382795.1:c.3591C>G NP_001369724.1:p.Phe1197Leu
NM_001382796.1:c.3552C>G NP_001369725.1:p.Phe1184Leu
NM_001382797.1:c.3540C>G NP_001369726.1:p.Phe1180Leu
NM_001382798.1:c.3483C>G NP_001369727.1:p.Phe1161Leu
NM_001382799.1:c.3459C>G NP_001369728.1:p.Phe1153Leu
NM_001382800.1:c.3453C>G NP_001369729.1:p.Phe1151Leu
NM_001382801.1:c.3435C>G NP_001369730.1:p.Phe1145Leu
NM_001382802.1:c.3381C>G NP_001369731.1:p.Phe1127Leu
NM_001382803.1:c.*218C>G NP_001369732.1:n.*218C>G
NM_001382804.1:c.2811C>G NP_001369733.1:p.Phe937Leu
NM_001382805.1:c.2688C>G NP_001369734.1:p.Phe896Leu
NM_001382806.1:c.2601C>G NP_001369735.1:p.Phe867Leu
NM_004448.4:c.3639C>G MANE Select NP_004439.2:p.Phe1213Leu
NR_110535.2:n.3877C>G