Canonical Allele Identifier: CA2259228812
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727448G= , CM000679.2:g.39727448G= GRCh38
NC_000017.10:g.37883701G= , CM000679.1:g.37883701G= GRCh37
NC_000017.9:g.35137227G= NCBI36
NG_007503.1:g.44309G= , LRG_724:g.44309G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3313G= MANE Select ENSP00000269571.4:p.Asp1105=
ENST00000269571.9:c.3313G= ENSP00000269571.4:p.Asp1105=
ENST00000406381.6:c.3223G= ENSP00000385185.2:p.Asp1075=
ENST00000445658.6:c.2485G= ENSP00000404047.2:p.Asp829=
ENST00000541774.5:c.3268G= ENSP00000446466.1:p.Asp1090=
ENST00000578373.5:c.*3103G= ENSP00000463427.1:n.*3103G=
ENST00000584450.5:c.3160-241G= ENSP00000463714.1:n.3160-241G=
ENST00000584601.5:c.3223G= ENSP00000462438.1:p.Asp1075=
NM_001005862.2:c.3223G= , LRG_724t1:c.3223G= NP_001005862.1:p.Asp1075=
NM_001289936.1:c.3268G= , LRG_724t4:c.3268G= NP_001276865.1:p.Asp1090=
NM_001289937.1:c.3160-241G= NP_001276866.1:n.3160-241G=
NM_004448.3:c.3313G= , LRG_724t2:c.3313G= NP_004439.2:p.Asp1105=
NR_110535.1:n.3637G=
XM_024450641.1:c.3451G= XP_024306409.1:p.Asp1151=
XM_024450642.1:c.3406G= XP_024306410.1:p.Asp1136=
XM_024450643.1:c.3361G= XP_024306411.1:p.Asp1121=
NM_001005862.3:c.3223G= NP_001005862.1:p.Asp1075=
NM_001289936.2:c.3268G= NP_001276865.1:p.Asp1090=
NM_001289937.2:c.3160-241G= NP_001276866.1:n.3160-241G=
NM_001382782.1:c.3223G= NP_001369711.1:p.Asp1075=
NM_001382783.1:c.3223G= NP_001369712.1:p.Asp1075=
NM_001382784.1:c.3430G= NP_001369713.1:p.Asp1144=
NM_001382785.1:c.3415G= NP_001369714.1:p.Asp1139=
NM_001382786.1:c.3394G= NP_001369715.1:p.Asp1132=
NM_001382787.1:c.3388G= NP_001369716.1:p.Asp1130=
NM_001382788.1:c.3343G= NP_001369717.1:p.Asp1115=
NM_001382789.1:c.3334G= NP_001369718.1:p.Asp1112=
NM_001382790.1:c.3310G= NP_001369719.1:p.Asp1104=
NM_001382791.1:c.3304G= NP_001369720.1:p.Asp1102=
NM_001382792.1:c.3277G= NP_001369721.1:p.Asp1093=
NM_001382793.1:c.3271G= NP_001369722.1:p.Asp1091=
NM_001382794.1:c.3271G= NP_001369723.1:p.Asp1091=
NM_001382795.1:c.3265G= NP_001369724.1:p.Asp1089=
NM_001382796.1:c.3226G= NP_001369725.1:p.Asp1076=
NM_001382797.1:c.3214G= NP_001369726.1:p.Asp1072=
NM_001382798.1:c.3157G= NP_001369727.1:p.Asp1053=
NM_001382799.1:c.3133G= NP_001369728.1:p.Asp1045=
NM_001382800.1:c.3127G= NP_001369729.1:p.Asp1043=
NM_001382801.1:c.3109G= NP_001369730.1:p.Asp1037=
NM_001382802.1:c.3055G= NP_001369731.1:p.Asp1019=
NM_001382803.1:c.3118-241G= NP_001369732.1:n.3118-241G=
NM_001382804.1:c.2485G= NP_001369733.1:p.Asp829=
NM_001382805.1:c.2362G= NP_001369734.1:p.Asp788=
NM_001382806.1:c.2275G= NP_001369735.1:p.Asp759=
NM_004448.4:c.3313G= MANE Select NP_004439.2:p.Asp1105=
NR_110535.2:n.3551G=