Canonical Allele Identifier: CA2259228685

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727341A= , CM000679.2:g.39727341A=	GRCh38
NC_000017.10:g.37883594A= , CM000679.1:g.37883594A=	GRCh37
NC_000017.9:g.35137120A=	NCBI36
NG_007503.1:g.44202A= , LRG_724:g.44202A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3206A= MANE Select	ENSP00000269571.4:p.Glu1069=
ENST00000269571.9:c.3206A=	ENSP00000269571.4:p.Glu1069=
ENST00000406381.6:c.3116A=	ENSP00000385185.2:p.Glu1039=
ENST00000445658.6:c.2378A=	ENSP00000404047.2:p.Glu793=
ENST00000541774.5:c.3161A=	ENSP00000446466.1:p.Glu1054=
ENST00000578373.5:c.*2996A=	ENSP00000463427.1:n.*2996A=
ENST00000584450.5:c.3159+338A=	ENSP00000463714.1:n.3159+338A=
ENST00000584601.5:c.3116A=	ENSP00000462438.1:p.Glu1039=
NM_001005862.2:c.3116A= , LRG_724t1:c.3116A=	NP_001005862.1:p.Glu1039=
NM_001289936.1:c.3161A= , LRG_724t4:c.3161A=	NP_001276865.1:p.Glu1054=
NM_001289937.1:c.3159+338A=	NP_001276866.1:n.3159+338A=
NM_004448.3:c.3206A= , LRG_724t2:c.3206A=	NP_004439.2:p.Glu1069=
NR_110535.1:n.3530A=
XM_024450641.1:c.3344A=	XP_024306409.1:p.Glu1115=
XM_024450642.1:c.3299A=	XP_024306410.1:p.Glu1100=
XM_024450643.1:c.3254A=	XP_024306411.1:p.Glu1085=
NM_001005862.3:c.3116A=	NP_001005862.1:p.Glu1039=
NM_001289936.2:c.3161A=	NP_001276865.1:p.Glu1054=
NM_001289937.2:c.3159+338A=	NP_001276866.1:n.3159+338A=
NM_001382782.1:c.3116A=	NP_001369711.1:p.Glu1039=
NM_001382783.1:c.3116A=	NP_001369712.1:p.Glu1039=
NM_001382784.1:c.3323A=	NP_001369713.1:p.Glu1108=
NM_001382785.1:c.3308A=	NP_001369714.1:p.Glu1103=
NM_001382786.1:c.3287A=	NP_001369715.1:p.Glu1096=
NM_001382787.1:c.3281A=	NP_001369716.1:p.Glu1094=
NM_001382788.1:c.3236A=	NP_001369717.1:p.Glu1079=
NM_001382789.1:c.3227A=	NP_001369718.1:p.Glu1076=
NM_001382790.1:c.3203A=	NP_001369719.1:p.Glu1068=
NM_001382791.1:c.3197A=	NP_001369720.1:p.Glu1066=
NM_001382792.1:c.3170A=	NP_001369721.1:p.Glu1057=
NM_001382793.1:c.3164A=	NP_001369722.1:p.Glu1055=
NM_001382794.1:c.3164A=	NP_001369723.1:p.Glu1055=
NM_001382795.1:c.3158A=	NP_001369724.1:p.Glu1053=
NM_001382796.1:c.3119A=	NP_001369725.1:p.Glu1040=
NM_001382797.1:c.3107A=	NP_001369726.1:p.Glu1036=
NM_001382798.1:c.3050A=	NP_001369727.1:p.Glu1017=
NM_001382799.1:c.3026A=	NP_001369728.1:p.Glu1009=
NM_001382800.1:c.3020A=	NP_001369729.1:p.Glu1007=
NM_001382801.1:c.3002A=	NP_001369730.1:p.Glu1001=
NM_001382802.1:c.2948A=	NP_001369731.1:p.Glu983=
NM_001382803.1:c.3117+338A=	NP_001369732.1:n.3117+338A=
NM_001382804.1:c.2378A=	NP_001369733.1:p.Glu793=
NM_001382805.1:c.2255A=	NP_001369734.1:p.Glu752=
NM_001382806.1:c.2168A=	NP_001369735.1:p.Glu723=
NM_004448.4:c.3206A= MANE Select	NP_004439.2:p.Glu1069=
NR_110535.2:n.3444A=