Canonical Allele Identifier: CA2259228823

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727467G= , CM000679.2:g.39727467G=	GRCh38
NC_000017.10:g.37883720G= , CM000679.1:g.37883720G=	GRCh37
NC_000017.9:g.35137246G=	NCBI36
NG_007503.1:g.44328G= , LRG_724:g.44328G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3332G= MANE Select	ENSP00000269571.4:p.Arg1111=
ENST00000269571.9:c.3332G=	ENSP00000269571.4:p.Arg1111=
ENST00000406381.6:c.3242G=	ENSP00000385185.2:p.Arg1081=
ENST00000445658.6:c.2504G=	ENSP00000404047.2:p.Arg835=
ENST00000541774.5:c.3287G=	ENSP00000446466.1:p.Arg1096=
ENST00000578373.5:c.*3122G=	ENSP00000463427.1:n.*3122G=
ENST00000584450.5:c.3160-222G=	ENSP00000463714.1:n.3160-222G=
ENST00000584601.5:c.3242G=	ENSP00000462438.1:p.Arg1081=
NM_001005862.2:c.3242G= , LRG_724t1:c.3242G=	NP_001005862.1:p.Arg1081=
NM_001289936.1:c.3287G= , LRG_724t4:c.3287G=	NP_001276865.1:p.Arg1096=
NM_001289937.1:c.3160-222G=	NP_001276866.1:n.3160-222G=
NM_004448.3:c.3332G= , LRG_724t2:c.3332G=	NP_004439.2:p.Arg1111=
NR_110535.1:n.3656G=
XM_024450641.1:c.3470G=	XP_024306409.1:p.Arg1157=
XM_024450642.1:c.3425G=	XP_024306410.1:p.Arg1142=
XM_024450643.1:c.3380G=	XP_024306411.1:p.Arg1127=
NM_001005862.3:c.3242G=	NP_001005862.1:p.Arg1081=
NM_001289936.2:c.3287G=	NP_001276865.1:p.Arg1096=
NM_001289937.2:c.3160-222G=	NP_001276866.1:n.3160-222G=
NM_001382782.1:c.3242G=	NP_001369711.1:p.Arg1081=
NM_001382783.1:c.3242G=	NP_001369712.1:p.Arg1081=
NM_001382784.1:c.3449G=	NP_001369713.1:p.Arg1150=
NM_001382785.1:c.3434G=	NP_001369714.1:p.Arg1145=
NM_001382786.1:c.3413G=	NP_001369715.1:p.Arg1138=
NM_001382787.1:c.3407G=	NP_001369716.1:p.Arg1136=
NM_001382788.1:c.3362G=	NP_001369717.1:p.Arg1121=
NM_001382789.1:c.3353G=	NP_001369718.1:p.Arg1118=
NM_001382790.1:c.3329G=	NP_001369719.1:p.Arg1110=
NM_001382791.1:c.3323G=	NP_001369720.1:p.Arg1108=
NM_001382792.1:c.3296G=	NP_001369721.1:p.Arg1099=
NM_001382793.1:c.3290G=	NP_001369722.1:p.Arg1097=
NM_001382794.1:c.3290G=	NP_001369723.1:p.Arg1097=
NM_001382795.1:c.3284G=	NP_001369724.1:p.Arg1095=
NM_001382796.1:c.3245G=	NP_001369725.1:p.Arg1082=
NM_001382797.1:c.3233G=	NP_001369726.1:p.Arg1078=
NM_001382798.1:c.3176G=	NP_001369727.1:p.Arg1059=
NM_001382799.1:c.3152G=	NP_001369728.1:p.Arg1051=
NM_001382800.1:c.3146G=	NP_001369729.1:p.Arg1049=
NM_001382801.1:c.3128G=	NP_001369730.1:p.Arg1043=
NM_001382802.1:c.3074G=	NP_001369731.1:p.Arg1025=
NM_001382803.1:c.3118-222G=	NP_001369732.1:n.3118-222G=
NM_001382804.1:c.2504G=	NP_001369733.1:p.Arg835=
NM_001382805.1:c.2381G=	NP_001369734.1:p.Arg794=
NM_001382806.1:c.2294G=	NP_001369735.1:p.Arg765=
NM_004448.4:c.3332G= MANE Select	NP_004439.2:p.Arg1111=
NR_110535.2:n.3570G=