Canonical Allele Identifier: CA2259228796

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727426G= , CM000679.2:g.39727426G=	GRCh38
NC_000017.10:g.37883679G= , CM000679.1:g.37883679G=	GRCh37
NC_000017.9:g.35137205G=	NCBI36
NG_007503.1:g.44287G= , LRG_724:g.44287G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3291G= MANE Select	ENSP00000269571.4:p.Gly1097=
ENST00000269571.9:c.3291G=	ENSP00000269571.4:p.Gly1097=
ENST00000406381.6:c.3201G=	ENSP00000385185.2:p.Gly1067=
ENST00000445658.6:c.2463G=	ENSP00000404047.2:p.Gly821=
ENST00000541774.5:c.3246G=	ENSP00000446466.1:p.Gly1082=
ENST00000578373.5:c.*3081G=	ENSP00000463427.1:n.*3081G=
ENST00000584450.5:c.3160-263G=	ENSP00000463714.1:n.3160-263G=
ENST00000584601.5:c.3201G=	ENSP00000462438.1:p.Gly1067=
NM_001005862.2:c.3201G= , LRG_724t1:c.3201G=	NP_001005862.1:p.Gly1067=
NM_001289936.1:c.3246G= , LRG_724t4:c.3246G=	NP_001276865.1:p.Gly1082=
NM_001289937.1:c.3160-263G=	NP_001276866.1:n.3160-263G=
NM_004448.3:c.3291G= , LRG_724t2:c.3291G=	NP_004439.2:p.Gly1097=
NR_110535.1:n.3615G=
XM_024450641.1:c.3429G=	XP_024306409.1:p.Gly1143=
XM_024450642.1:c.3384G=	XP_024306410.1:p.Gly1128=
XM_024450643.1:c.3339G=	XP_024306411.1:p.Gly1113=
NM_001005862.3:c.3201G=	NP_001005862.1:p.Gly1067=
NM_001289936.2:c.3246G=	NP_001276865.1:p.Gly1082=
NM_001289937.2:c.3160-263G=	NP_001276866.1:n.3160-263G=
NM_001382782.1:c.3201G=	NP_001369711.1:p.Gly1067=
NM_001382783.1:c.3201G=	NP_001369712.1:p.Gly1067=
NM_001382784.1:c.3408G=	NP_001369713.1:p.Gly1136=
NM_001382785.1:c.3393G=	NP_001369714.1:p.Gly1131=
NM_001382786.1:c.3372G=	NP_001369715.1:p.Gly1124=
NM_001382787.1:c.3366G=	NP_001369716.1:p.Gly1122=
NM_001382788.1:c.3321G=	NP_001369717.1:p.Gly1107=
NM_001382789.1:c.3312G=	NP_001369718.1:p.Gly1104=
NM_001382790.1:c.3288G=	NP_001369719.1:p.Gly1096=
NM_001382791.1:c.3282G=	NP_001369720.1:p.Gly1094=
NM_001382792.1:c.3255G=	NP_001369721.1:p.Gly1085=
NM_001382793.1:c.3249G=	NP_001369722.1:p.Gly1083=
NM_001382794.1:c.3249G=	NP_001369723.1:p.Gly1083=
NM_001382795.1:c.3243G=	NP_001369724.1:p.Gly1081=
NM_001382796.1:c.3204G=	NP_001369725.1:p.Gly1068=
NM_001382797.1:c.3192G=	NP_001369726.1:p.Gly1064=
NM_001382798.1:c.3135G=	NP_001369727.1:p.Gly1045=
NM_001382799.1:c.3111G=	NP_001369728.1:p.Gly1037=
NM_001382800.1:c.3105G=	NP_001369729.1:p.Gly1035=
NM_001382801.1:c.3087G=	NP_001369730.1:p.Gly1029=
NM_001382802.1:c.3033G=	NP_001369731.1:p.Gly1011=
NM_001382803.1:c.3118-263G=	NP_001369732.1:n.3118-263G=
NM_001382804.1:c.2463G=	NP_001369733.1:p.Gly821=
NM_001382805.1:c.2340G=	NP_001369734.1:p.Gly780=
NM_001382806.1:c.2253G=	NP_001369735.1:p.Gly751=
NM_004448.4:c.3291G= MANE Select	NP_004439.2:p.Gly1097=
NR_110535.2:n.3529G=