Canonical Allele Identifier: CA2259229152
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727542A= , CM000679.2:g.39727542A= GRCh38
NC_000017.10:g.37883795A= , CM000679.1:g.37883795A= GRCh37
NC_000017.9:g.35137321A= NCBI36
NG_007503.1:g.44403A= , LRG_724:g.44403A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3407A= MANE Select ENSP00000269571.4:p.Gln1136=
ENST00000269571.9:c.3407A= ENSP00000269571.4:p.Gln1136=
ENST00000406381.6:c.3317A= ENSP00000385185.2:p.Gln1106=
ENST00000445658.6:c.2579A= ENSP00000404047.2:p.Gln860=
ENST00000541774.5:c.3362A= ENSP00000446466.1:p.Gln1121=
ENST00000578373.5:c.*3197A= ENSP00000463427.1:n.*3197A=
ENST00000584450.5:c.3160-147A= ENSP00000463714.1:n.3160-147A=
ENST00000584601.5:c.3317A= ENSP00000462438.1:p.Gln1106=
NM_001005862.2:c.3317A= , LRG_724t1:c.3317A= NP_001005862.1:p.Gln1106=
NM_001289936.1:c.3362A= , LRG_724t4:c.3362A= NP_001276865.1:p.Gln1121=
NM_001289937.1:c.3160-147A= NP_001276866.1:n.3160-147A=
NM_004448.3:c.3407A= , LRG_724t2:c.3407A= NP_004439.2:p.Gln1136=
NR_110535.1:n.3731A=
XM_024450641.1:c.3545A= XP_024306409.1:p.Gln1182=
XM_024450642.1:c.3500A= XP_024306410.1:p.Gln1167=
XM_024450643.1:c.3455A= XP_024306411.1:p.Gln1152=
NM_001005862.3:c.3317A= NP_001005862.1:p.Gln1106=
NM_001289936.2:c.3362A= NP_001276865.1:p.Gln1121=
NM_001289937.2:c.3160-147A= NP_001276866.1:n.3160-147A=
NM_001382782.1:c.3317A= NP_001369711.1:p.Gln1106=
NM_001382783.1:c.3317A= NP_001369712.1:p.Gln1106=
NM_001382784.1:c.3524A= NP_001369713.1:p.Gln1175=
NM_001382785.1:c.3509A= NP_001369714.1:p.Gln1170=
NM_001382786.1:c.3488A= NP_001369715.1:p.Gln1163=
NM_001382787.1:c.3482A= NP_001369716.1:p.Gln1161=
NM_001382788.1:c.3437A= NP_001369717.1:p.Gln1146=
NM_001382789.1:c.3428A= NP_001369718.1:p.Gln1143=
NM_001382790.1:c.3404A= NP_001369719.1:p.Gln1135=
NM_001382791.1:c.3398A= NP_001369720.1:p.Gln1133=
NM_001382792.1:c.3371A= NP_001369721.1:p.Gln1124=
NM_001382793.1:c.3365A= NP_001369722.1:p.Gln1122=
NM_001382794.1:c.3365A= NP_001369723.1:p.Gln1122=
NM_001382795.1:c.3359A= NP_001369724.1:p.Gln1120=
NM_001382796.1:c.3320A= NP_001369725.1:p.Gln1107=
NM_001382797.1:c.3308A= NP_001369726.1:p.Gln1103=
NM_001382798.1:c.3251A= NP_001369727.1:p.Gln1084=
NM_001382799.1:c.3227A= NP_001369728.1:p.Gln1076=
NM_001382800.1:c.3221A= NP_001369729.1:p.Gln1074=
NM_001382801.1:c.3203A= NP_001369730.1:p.Gln1068=
NM_001382802.1:c.3149A= NP_001369731.1:p.Gln1050=
NM_001382803.1:c.3118-147A= NP_001369732.1:n.3118-147A=
NM_001382804.1:c.2579A= NP_001369733.1:p.Gln860=
NM_001382805.1:c.2456A= NP_001369734.1:p.Gln819=
NM_001382806.1:c.2369A= NP_001369735.1:p.Gln790=
NM_004448.4:c.3407A= MANE Select NP_004439.2:p.Gln1136=
NR_110535.2:n.3645A=