Canonical Allele Identifier: CA2259228739

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727381C= , CM000679.2:g.39727381C=	GRCh38
NC_000017.10:g.37883634C= , CM000679.1:g.37883634C=	GRCh37
NC_000017.9:g.35137160C=	NCBI36
NG_007503.1:g.44242C= , LRG_724:g.44242C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3246C= MANE Select	ENSP00000269571.4:p.Gly1082=
ENST00000269571.9:c.3246C=	ENSP00000269571.4:p.Gly1082=
ENST00000406381.6:c.3156C=	ENSP00000385185.2:p.Gly1052=
ENST00000445658.6:c.2418C=	ENSP00000404047.2:p.Gly806=
ENST00000541774.5:c.3201C=	ENSP00000446466.1:p.Gly1067=
ENST00000578373.5:c.*3036C=	ENSP00000463427.1:n.*3036C=
ENST00000584450.5:c.3160-308C=	ENSP00000463714.1:n.3160-308C=
ENST00000584601.5:c.3156C=	ENSP00000462438.1:p.Gly1052=
NM_001005862.2:c.3156C= , LRG_724t1:c.3156C=	NP_001005862.1:p.Gly1052=
NM_001289936.1:c.3201C= , LRG_724t4:c.3201C=	NP_001276865.1:p.Gly1067=
NM_001289937.1:c.3160-308C=	NP_001276866.1:n.3160-308C=
NM_004448.3:c.3246C= , LRG_724t2:c.3246C=	NP_004439.2:p.Gly1082=
NR_110535.1:n.3570C=
XM_024450641.1:c.3384C=	XP_024306409.1:p.Gly1128=
XM_024450642.1:c.3339C=	XP_024306410.1:p.Gly1113=
XM_024450643.1:c.3294C=	XP_024306411.1:p.Gly1098=
NM_001005862.3:c.3156C=	NP_001005862.1:p.Gly1052=
NM_001289936.2:c.3201C=	NP_001276865.1:p.Gly1067=
NM_001289937.2:c.3160-308C=	NP_001276866.1:n.3160-308C=
NM_001382782.1:c.3156C=	NP_001369711.1:p.Gly1052=
NM_001382783.1:c.3156C=	NP_001369712.1:p.Gly1052=
NM_001382784.1:c.3363C=	NP_001369713.1:p.Gly1121=
NM_001382785.1:c.3348C=	NP_001369714.1:p.Gly1116=
NM_001382786.1:c.3327C=	NP_001369715.1:p.Gly1109=
NM_001382787.1:c.3321C=	NP_001369716.1:p.Gly1107=
NM_001382788.1:c.3276C=	NP_001369717.1:p.Gly1092=
NM_001382789.1:c.3267C=	NP_001369718.1:p.Gly1089=
NM_001382790.1:c.3243C=	NP_001369719.1:p.Gly1081=
NM_001382791.1:c.3237C=	NP_001369720.1:p.Gly1079=
NM_001382792.1:c.3210C=	NP_001369721.1:p.Gly1070=
NM_001382793.1:c.3204C=	NP_001369722.1:p.Gly1068=
NM_001382794.1:c.3204C=	NP_001369723.1:p.Gly1068=
NM_001382795.1:c.3198C=	NP_001369724.1:p.Gly1066=
NM_001382796.1:c.3159C=	NP_001369725.1:p.Gly1053=
NM_001382797.1:c.3147C=	NP_001369726.1:p.Gly1049=
NM_001382798.1:c.3090C=	NP_001369727.1:p.Gly1030=
NM_001382799.1:c.3066C=	NP_001369728.1:p.Gly1022=
NM_001382800.1:c.3060C=	NP_001369729.1:p.Gly1020=
NM_001382801.1:c.3042C=	NP_001369730.1:p.Gly1014=
NM_001382802.1:c.2988C=	NP_001369731.1:p.Gly996=
NM_001382803.1:c.3118-308C=	NP_001369732.1:n.3118-308C=
NM_001382804.1:c.2418C=	NP_001369733.1:p.Gly806=
NM_001382805.1:c.2295C=	NP_001369734.1:p.Gly765=
NM_001382806.1:c.2208C=	NP_001369735.1:p.Gly736=
NM_004448.4:c.3246C= MANE Select	NP_004439.2:p.Gly1082=
NR_110535.2:n.3484C=