Canonical Allele Identifier: CA2259228800
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727434G= , CM000679.2:g.39727434G= GRCh38
NC_000017.10:g.37883687G= , CM000679.1:g.37883687G= GRCh37
NC_000017.9:g.35137213G= NCBI36
NG_007503.1:g.44295G= , LRG_724:g.44295G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3299G= MANE Select ENSP00000269571.4:p.Ser1100=
ENST00000269571.9:c.3299G= ENSP00000269571.4:p.Ser1100=
ENST00000406381.6:c.3209G= ENSP00000385185.2:p.Ser1070=
ENST00000445658.6:c.2471G= ENSP00000404047.2:p.Ser824=
ENST00000541774.5:c.3254G= ENSP00000446466.1:p.Ser1085=
ENST00000578373.5:c.*3089G= ENSP00000463427.1:n.*3089G=
ENST00000584450.5:c.3160-255G= ENSP00000463714.1:n.3160-255G=
ENST00000584601.5:c.3209G= ENSP00000462438.1:p.Ser1070=
NM_001005862.2:c.3209G= , LRG_724t1:c.3209G= NP_001005862.1:p.Ser1070=
NM_001289936.1:c.3254G= , LRG_724t4:c.3254G= NP_001276865.1:p.Ser1085=
NM_001289937.1:c.3160-255G= NP_001276866.1:n.3160-255G=
NM_004448.3:c.3299G= , LRG_724t2:c.3299G= NP_004439.2:p.Ser1100=
NR_110535.1:n.3623G=
XM_024450641.1:c.3437G= XP_024306409.1:p.Ser1146=
XM_024450642.1:c.3392G= XP_024306410.1:p.Ser1131=
XM_024450643.1:c.3347G= XP_024306411.1:p.Ser1116=
NM_001005862.3:c.3209G= NP_001005862.1:p.Ser1070=
NM_001289936.2:c.3254G= NP_001276865.1:p.Ser1085=
NM_001289937.2:c.3160-255G= NP_001276866.1:n.3160-255G=
NM_001382782.1:c.3209G= NP_001369711.1:p.Ser1070=
NM_001382783.1:c.3209G= NP_001369712.1:p.Ser1070=
NM_001382784.1:c.3416G= NP_001369713.1:p.Ser1139=
NM_001382785.1:c.3401G= NP_001369714.1:p.Ser1134=
NM_001382786.1:c.3380G= NP_001369715.1:p.Ser1127=
NM_001382787.1:c.3374G= NP_001369716.1:p.Ser1125=
NM_001382788.1:c.3329G= NP_001369717.1:p.Ser1110=
NM_001382789.1:c.3320G= NP_001369718.1:p.Ser1107=
NM_001382790.1:c.3296G= NP_001369719.1:p.Ser1099=
NM_001382791.1:c.3290G= NP_001369720.1:p.Ser1097=
NM_001382792.1:c.3263G= NP_001369721.1:p.Ser1088=
NM_001382793.1:c.3257G= NP_001369722.1:p.Ser1086=
NM_001382794.1:c.3257G= NP_001369723.1:p.Ser1086=
NM_001382795.1:c.3251G= NP_001369724.1:p.Ser1084=
NM_001382796.1:c.3212G= NP_001369725.1:p.Ser1071=
NM_001382797.1:c.3200G= NP_001369726.1:p.Ser1067=
NM_001382798.1:c.3143G= NP_001369727.1:p.Ser1048=
NM_001382799.1:c.3119G= NP_001369728.1:p.Ser1040=
NM_001382800.1:c.3113G= NP_001369729.1:p.Ser1038=
NM_001382801.1:c.3095G= NP_001369730.1:p.Ser1032=
NM_001382802.1:c.3041G= NP_001369731.1:p.Ser1014=
NM_001382803.1:c.3118-255G= NP_001369732.1:n.3118-255G=
NM_001382804.1:c.2471G= NP_001369733.1:p.Ser824=
NM_001382805.1:c.2348G= NP_001369734.1:p.Ser783=
NM_001382806.1:c.2261G= NP_001369735.1:p.Ser754=
NM_004448.4:c.3299G= MANE Select NP_004439.2:p.Ser1100=
NR_110535.2:n.3537G=