Canonical Allele Identifier: CA2259229281
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727832G= , CM000679.2:g.39727832G= GRCh38
NC_000017.10:g.37884085G= , CM000679.1:g.37884085G= GRCh37
NC_000017.9:g.35137611G= NCBI36
NG_007503.1:g.44693G= , LRG_724:g.44693G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3556G= MANE Select ENSP00000269571.4:p.Ala1186=
ENST00000269571.9:c.3556G= ENSP00000269571.4:p.Ala1186=
ENST00000406381.6:c.3466G= ENSP00000385185.2:p.Ala1156=
ENST00000445658.6:c.2728G= ENSP00000404047.2:p.Ala910=
ENST00000541774.5:c.3511G= ENSP00000446466.1:p.Ala1171=
ENST00000578373.5:c.*3346G= ENSP00000463427.1:n.*3346G=
ENST00000584450.5:c.*135G= ENSP00000463714.1:n.*135G=
ENST00000584601.5:c.3466G= ENSP00000462438.1:p.Ala1156=
NM_001005862.2:c.3466G= , LRG_724t1:c.3466G= NP_001005862.1:p.Ala1156=
NM_001289936.1:c.3511G= , LRG_724t4:c.3511G= NP_001276865.1:p.Ala1171=
NM_001289937.1:c.*135G= NP_001276866.1:n.*135G=
NM_004448.3:c.3556G= , LRG_724t2:c.3556G= NP_004439.2:p.Ala1186=
NR_110535.1:n.3880G=
XM_024450641.1:c.3694G= XP_024306409.1:p.Ala1232=
XM_024450642.1:c.3649G= XP_024306410.1:p.Ala1217=
XM_024450643.1:c.3604G= XP_024306411.1:p.Ala1202=
NM_001005862.3:c.3466G= NP_001005862.1:p.Ala1156=
NM_001289936.2:c.3511G= NP_001276865.1:p.Ala1171=
NM_001289937.2:c.*135G= NP_001276866.1:n.*135G=
NM_001382782.1:c.3466G= NP_001369711.1:p.Ala1156=
NM_001382783.1:c.3466G= NP_001369712.1:p.Ala1156=
NM_001382784.1:c.3673G= NP_001369713.1:p.Ala1225=
NM_001382785.1:c.3658G= NP_001369714.1:p.Ala1220=
NM_001382786.1:c.3637G= NP_001369715.1:p.Ala1213=
NM_001382787.1:c.3631G= NP_001369716.1:p.Ala1211=
NM_001382788.1:c.3586G= NP_001369717.1:p.Ala1196=
NM_001382789.1:c.3577G= NP_001369718.1:p.Ala1193=
NM_001382790.1:c.3553G= NP_001369719.1:p.Ala1185=
NM_001382791.1:c.3547G= NP_001369720.1:p.Ala1183=
NM_001382792.1:c.3520G= NP_001369721.1:p.Ala1174=
NM_001382793.1:c.3514G= NP_001369722.1:p.Ala1172=
NM_001382794.1:c.3514G= NP_001369723.1:p.Ala1172=
NM_001382795.1:c.3508G= NP_001369724.1:p.Ala1170=
NM_001382796.1:c.3469G= NP_001369725.1:p.Ala1157=
NM_001382797.1:c.3457G= NP_001369726.1:p.Ala1153=
NM_001382798.1:c.3400G= NP_001369727.1:p.Ala1134=
NM_001382799.1:c.3376G= NP_001369728.1:p.Ala1126=
NM_001382800.1:c.3370G= NP_001369729.1:p.Ala1124=
NM_001382801.1:c.3352G= NP_001369730.1:p.Ala1118=
NM_001382802.1:c.3298G= NP_001369731.1:p.Ala1100=
NM_001382803.1:c.*135G= NP_001369732.1:n.*135G=
NM_001382804.1:c.2728G= NP_001369733.1:p.Ala910=
NM_001382805.1:c.2605G= NP_001369734.1:p.Ala869=
NM_001382806.1:c.2518G= NP_001369735.1:p.Ala840=
NM_004448.4:c.3556G= MANE Select NP_004439.2:p.Ala1186=
NR_110535.2:n.3794G=