Canonical Allele Identifier: CA2259228825
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727472A= , CM000679.2:g.39727472A= GRCh38
NC_000017.10:g.37883725A= , CM000679.1:g.37883725A= GRCh37
NC_000017.9:g.35137251A= NCBI36
NG_007503.1:g.44333A= , LRG_724:g.44333A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3337A= MANE Select ENSP00000269571.4:p.Ser1113=
ENST00000269571.9:c.3337A= ENSP00000269571.4:p.Ser1113=
ENST00000406381.6:c.3247A= ENSP00000385185.2:p.Ser1083=
ENST00000445658.6:c.2509A= ENSP00000404047.2:p.Ser837=
ENST00000541774.5:c.3292A= ENSP00000446466.1:p.Ser1098=
ENST00000578373.5:c.*3127A= ENSP00000463427.1:n.*3127A=
ENST00000584450.5:c.3160-217A= ENSP00000463714.1:n.3160-217A=
ENST00000584601.5:c.3247A= ENSP00000462438.1:p.Ser1083=
NM_001005862.2:c.3247A= , LRG_724t1:c.3247A= NP_001005862.1:p.Ser1083=
NM_001289936.1:c.3292A= , LRG_724t4:c.3292A= NP_001276865.1:p.Ser1098=
NM_001289937.1:c.3160-217A= NP_001276866.1:n.3160-217A=
NM_004448.3:c.3337A= , LRG_724t2:c.3337A= NP_004439.2:p.Ser1113=
NR_110535.1:n.3661A=
XM_024450641.1:c.3475A= XP_024306409.1:p.Ser1159=
XM_024450642.1:c.3430A= XP_024306410.1:p.Ser1144=
XM_024450643.1:c.3385A= XP_024306411.1:p.Ser1129=
NM_001005862.3:c.3247A= NP_001005862.1:p.Ser1083=
NM_001289936.2:c.3292A= NP_001276865.1:p.Ser1098=
NM_001289937.2:c.3160-217A= NP_001276866.1:n.3160-217A=
NM_001382782.1:c.3247A= NP_001369711.1:p.Ser1083=
NM_001382783.1:c.3247A= NP_001369712.1:p.Ser1083=
NM_001382784.1:c.3454A= NP_001369713.1:p.Ser1152=
NM_001382785.1:c.3439A= NP_001369714.1:p.Ser1147=
NM_001382786.1:c.3418A= NP_001369715.1:p.Ser1140=
NM_001382787.1:c.3412A= NP_001369716.1:p.Ser1138=
NM_001382788.1:c.3367A= NP_001369717.1:p.Ser1123=
NM_001382789.1:c.3358A= NP_001369718.1:p.Ser1120=
NM_001382790.1:c.3334A= NP_001369719.1:p.Ser1112=
NM_001382791.1:c.3328A= NP_001369720.1:p.Ser1110=
NM_001382792.1:c.3301A= NP_001369721.1:p.Ser1101=
NM_001382793.1:c.3295A= NP_001369722.1:p.Ser1099=
NM_001382794.1:c.3295A= NP_001369723.1:p.Ser1099=
NM_001382795.1:c.3289A= NP_001369724.1:p.Ser1097=
NM_001382796.1:c.3250A= NP_001369725.1:p.Ser1084=
NM_001382797.1:c.3238A= NP_001369726.1:p.Ser1080=
NM_001382798.1:c.3181A= NP_001369727.1:p.Ser1061=
NM_001382799.1:c.3157A= NP_001369728.1:p.Ser1053=
NM_001382800.1:c.3151A= NP_001369729.1:p.Ser1051=
NM_001382801.1:c.3133A= NP_001369730.1:p.Ser1045=
NM_001382802.1:c.3079A= NP_001369731.1:p.Ser1027=
NM_001382803.1:c.3118-217A= NP_001369732.1:n.3118-217A=
NM_001382804.1:c.2509A= NP_001369733.1:p.Ser837=
NM_001382805.1:c.2386A= NP_001369734.1:p.Ser796=
NM_001382806.1:c.2299A= NP_001369735.1:p.Ser767=
NM_004448.4:c.3337A= MANE Select NP_004439.2:p.Ser1113=
NR_110535.2:n.3575A=