Canonical Allele Identifier: CA2259228831

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727479A= , CM000679.2:g.39727479A=	GRCh38
NC_000017.10:g.37883732A= , CM000679.1:g.37883732A=	GRCh37
NC_000017.9:g.35137258A=	NCBI36
NG_007503.1:g.44340A= , LRG_724:g.44340A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3344A= MANE Select	ENSP00000269571.4:p.Asp1115=
ENST00000269571.9:c.3344A=	ENSP00000269571.4:p.Asp1115=
ENST00000406381.6:c.3254A=	ENSP00000385185.2:p.Asp1085=
ENST00000445658.6:c.2516A=	ENSP00000404047.2:p.Asp839=
ENST00000541774.5:c.3299A=	ENSP00000446466.1:p.Asp1100=
ENST00000578373.5:c.*3134A=	ENSP00000463427.1:n.*3134A=
ENST00000584450.5:c.3160-210A=	ENSP00000463714.1:n.3160-210A=
ENST00000584601.5:c.3254A=	ENSP00000462438.1:p.Asp1085=
NM_001005862.2:c.3254A= , LRG_724t1:c.3254A=	NP_001005862.1:p.Asp1085=
NM_001289936.1:c.3299A= , LRG_724t4:c.3299A=	NP_001276865.1:p.Asp1100=
NM_001289937.1:c.3160-210A=	NP_001276866.1:n.3160-210A=
NM_004448.3:c.3344A= , LRG_724t2:c.3344A=	NP_004439.2:p.Asp1115=
NR_110535.1:n.3668A=
XM_024450641.1:c.3482A=	XP_024306409.1:p.Asp1161=
XM_024450642.1:c.3437A=	XP_024306410.1:p.Asp1146=
XM_024450643.1:c.3392A=	XP_024306411.1:p.Asp1131=
NM_001005862.3:c.3254A=	NP_001005862.1:p.Asp1085=
NM_001289936.2:c.3299A=	NP_001276865.1:p.Asp1100=
NM_001289937.2:c.3160-210A=	NP_001276866.1:n.3160-210A=
NM_001382782.1:c.3254A=	NP_001369711.1:p.Asp1085=
NM_001382783.1:c.3254A=	NP_001369712.1:p.Asp1085=
NM_001382784.1:c.3461A=	NP_001369713.1:p.Asp1154=
NM_001382785.1:c.3446A=	NP_001369714.1:p.Asp1149=
NM_001382786.1:c.3425A=	NP_001369715.1:p.Asp1142=
NM_001382787.1:c.3419A=	NP_001369716.1:p.Asp1140=
NM_001382788.1:c.3374A=	NP_001369717.1:p.Asp1125=
NM_001382789.1:c.3365A=	NP_001369718.1:p.Asp1122=
NM_001382790.1:c.3341A=	NP_001369719.1:p.Asp1114=
NM_001382791.1:c.3335A=	NP_001369720.1:p.Asp1112=
NM_001382792.1:c.3308A=	NP_001369721.1:p.Asp1103=
NM_001382793.1:c.3302A=	NP_001369722.1:p.Asp1101=
NM_001382794.1:c.3302A=	NP_001369723.1:p.Asp1101=
NM_001382795.1:c.3296A=	NP_001369724.1:p.Asp1099=
NM_001382796.1:c.3257A=	NP_001369725.1:p.Asp1086=
NM_001382797.1:c.3245A=	NP_001369726.1:p.Asp1082=
NM_001382798.1:c.3188A=	NP_001369727.1:p.Asp1063=
NM_001382799.1:c.3164A=	NP_001369728.1:p.Asp1055=
NM_001382800.1:c.3158A=	NP_001369729.1:p.Asp1053=
NM_001382801.1:c.3140A=	NP_001369730.1:p.Asp1047=
NM_001382802.1:c.3086A=	NP_001369731.1:p.Asp1029=
NM_001382803.1:c.3118-210A=	NP_001369732.1:n.3118-210A=
NM_001382804.1:c.2516A=	NP_001369733.1:p.Asp839=
NM_001382805.1:c.2393A=	NP_001369734.1:p.Asp798=
NM_001382806.1:c.2306A=	NP_001369735.1:p.Asp769=
NM_004448.4:c.3344A= MANE Select	NP_004439.2:p.Asp1115=
NR_110535.2:n.3582A=