Canonical Allele Identifier: CA2259228677

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727334G= , CM000679.2:g.39727334G=	GRCh38
NC_000017.10:g.37883587G= , CM000679.1:g.37883587G=	GRCh37
NC_000017.9:g.35137113G=	NCBI36
NG_007503.1:g.44195G= , LRG_724:g.44195G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3199G= MANE Select	ENSP00000269571.4:p.Glu1067=
ENST00000269571.9:c.3199G=	ENSP00000269571.4:p.Glu1067=
ENST00000406381.6:c.3109G=	ENSP00000385185.2:p.Glu1037=
ENST00000445658.6:c.2371G=	ENSP00000404047.2:p.Glu791=
ENST00000541774.5:c.3154G=	ENSP00000446466.1:p.Glu1052=
ENST00000578373.5:c.*2989G=	ENSP00000463427.1:n.*2989G=
ENST00000584450.5:c.3159+331G=	ENSP00000463714.1:n.3159+331G=
ENST00000584601.5:c.3109G=	ENSP00000462438.1:p.Glu1037=
NM_001005862.2:c.3109G= , LRG_724t1:c.3109G=	NP_001005862.1:p.Glu1037=
NM_001289936.1:c.3154G= , LRG_724t4:c.3154G=	NP_001276865.1:p.Glu1052=
NM_001289937.1:c.3159+331G=	NP_001276866.1:n.3159+331G=
NM_004448.3:c.3199G= , LRG_724t2:c.3199G=	NP_004439.2:p.Glu1067=
NR_110535.1:n.3523G=
XM_024450641.1:c.3337G=	XP_024306409.1:p.Glu1113=
XM_024450642.1:c.3292G=	XP_024306410.1:p.Glu1098=
XM_024450643.1:c.3247G=	XP_024306411.1:p.Glu1083=
NM_001005862.3:c.3109G=	NP_001005862.1:p.Glu1037=
NM_001289936.2:c.3154G=	NP_001276865.1:p.Glu1052=
NM_001289937.2:c.3159+331G=	NP_001276866.1:n.3159+331G=
NM_001382782.1:c.3109G=	NP_001369711.1:p.Glu1037=
NM_001382783.1:c.3109G=	NP_001369712.1:p.Glu1037=
NM_001382784.1:c.3316G=	NP_001369713.1:p.Glu1106=
NM_001382785.1:c.3301G=	NP_001369714.1:p.Glu1101=
NM_001382786.1:c.3280G=	NP_001369715.1:p.Glu1094=
NM_001382787.1:c.3274G=	NP_001369716.1:p.Glu1092=
NM_001382788.1:c.3229G=	NP_001369717.1:p.Glu1077=
NM_001382789.1:c.3220G=	NP_001369718.1:p.Glu1074=
NM_001382790.1:c.3196G=	NP_001369719.1:p.Glu1066=
NM_001382791.1:c.3190G=	NP_001369720.1:p.Glu1064=
NM_001382792.1:c.3163G=	NP_001369721.1:p.Glu1055=
NM_001382793.1:c.3157G=	NP_001369722.1:p.Glu1053=
NM_001382794.1:c.3157G=	NP_001369723.1:p.Glu1053=
NM_001382795.1:c.3151G=	NP_001369724.1:p.Glu1051=
NM_001382796.1:c.3112G=	NP_001369725.1:p.Glu1038=
NM_001382797.1:c.3100G=	NP_001369726.1:p.Glu1034=
NM_001382798.1:c.3043G=	NP_001369727.1:p.Glu1015=
NM_001382799.1:c.3019G=	NP_001369728.1:p.Glu1007=
NM_001382800.1:c.3013G=	NP_001369729.1:p.Glu1005=
NM_001382801.1:c.2995G=	NP_001369730.1:p.Glu999=
NM_001382802.1:c.2941G=	NP_001369731.1:p.Glu981=
NM_001382803.1:c.3117+331G=	NP_001369732.1:n.3117+331G=
NM_001382804.1:c.2371G=	NP_001369733.1:p.Glu791=
NM_001382805.1:c.2248G=	NP_001369734.1:p.Glu750=
NM_001382806.1:c.2161G=	NP_001369735.1:p.Glu721=
NM_004448.4:c.3199G= MANE Select	NP_004439.2:p.Glu1067=
NR_110535.2:n.3437G=