Canonical Allele Identifier: CA2259229140
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727516C= , CM000679.2:g.39727516C= GRCh38
NC_000017.10:g.37883769C= , CM000679.1:g.37883769C= GRCh37
NC_000017.9:g.35137295C= NCBI36
NG_007503.1:g.44377C= , LRG_724:g.44377C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3381C= MANE Select ENSP00000269571.4:p.Tyr1127=
ENST00000269571.9:c.3381C= ENSP00000269571.4:p.Tyr1127=
ENST00000406381.6:c.3291C= ENSP00000385185.2:p.Tyr1097=
ENST00000445658.6:c.2553C= ENSP00000404047.2:p.Tyr851=
ENST00000541774.5:c.3336C= ENSP00000446466.1:p.Tyr1112=
ENST00000578373.5:c.*3171C= ENSP00000463427.1:n.*3171C=
ENST00000584450.5:c.3160-173C= ENSP00000463714.1:n.3160-173C=
ENST00000584601.5:c.3291C= ENSP00000462438.1:p.Tyr1097=
NM_001005862.2:c.3291C= , LRG_724t1:c.3291C= NP_001005862.1:p.Tyr1097=
NM_001289936.1:c.3336C= , LRG_724t4:c.3336C= NP_001276865.1:p.Tyr1112=
NM_001289937.1:c.3160-173C= NP_001276866.1:n.3160-173C=
NM_004448.3:c.3381C= , LRG_724t2:c.3381C= NP_004439.2:p.Tyr1127=
NR_110535.1:n.3705C=
XM_024450641.1:c.3519C= XP_024306409.1:p.Tyr1173=
XM_024450642.1:c.3474C= XP_024306410.1:p.Tyr1158=
XM_024450643.1:c.3429C= XP_024306411.1:p.Tyr1143=
NM_001005862.3:c.3291C= NP_001005862.1:p.Tyr1097=
NM_001289936.2:c.3336C= NP_001276865.1:p.Tyr1112=
NM_001289937.2:c.3160-173C= NP_001276866.1:n.3160-173C=
NM_001382782.1:c.3291C= NP_001369711.1:p.Tyr1097=
NM_001382783.1:c.3291C= NP_001369712.1:p.Tyr1097=
NM_001382784.1:c.3498C= NP_001369713.1:p.Tyr1166=
NM_001382785.1:c.3483C= NP_001369714.1:p.Tyr1161=
NM_001382786.1:c.3462C= NP_001369715.1:p.Tyr1154=
NM_001382787.1:c.3456C= NP_001369716.1:p.Tyr1152=
NM_001382788.1:c.3411C= NP_001369717.1:p.Tyr1137=
NM_001382789.1:c.3402C= NP_001369718.1:p.Tyr1134=
NM_001382790.1:c.3378C= NP_001369719.1:p.Tyr1126=
NM_001382791.1:c.3372C= NP_001369720.1:p.Tyr1124=
NM_001382792.1:c.3345C= NP_001369721.1:p.Tyr1115=
NM_001382793.1:c.3339C= NP_001369722.1:p.Tyr1113=
NM_001382794.1:c.3339C= NP_001369723.1:p.Tyr1113=
NM_001382795.1:c.3333C= NP_001369724.1:p.Tyr1111=
NM_001382796.1:c.3294C= NP_001369725.1:p.Tyr1098=
NM_001382797.1:c.3282C= NP_001369726.1:p.Tyr1094=
NM_001382798.1:c.3225C= NP_001369727.1:p.Tyr1075=
NM_001382799.1:c.3201C= NP_001369728.1:p.Tyr1067=
NM_001382800.1:c.3195C= NP_001369729.1:p.Tyr1065=
NM_001382801.1:c.3177C= NP_001369730.1:p.Tyr1059=
NM_001382802.1:c.3123C= NP_001369731.1:p.Tyr1041=
NM_001382803.1:c.3118-173C= NP_001369732.1:n.3118-173C=
NM_001382804.1:c.2553C= NP_001369733.1:p.Tyr851=
NM_001382805.1:c.2430C= NP_001369734.1:p.Tyr810=
NM_001382806.1:c.2343C= NP_001369735.1:p.Tyr781=
NM_004448.4:c.3381C= MANE Select NP_004439.2:p.Tyr1127=
NR_110535.2:n.3619C=