Canonical Allele Identifier: CA2259228766

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727398G= , CM000679.2:g.39727398G=	GRCh38
NC_000017.10:g.37883651G= , CM000679.1:g.37883651G=	GRCh37
NC_000017.9:g.35137177G=	NCBI36
NG_007503.1:g.44259G= , LRG_724:g.44259G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3263G= MANE Select	ENSP00000269571.4:p.Gly1088=
ENST00000269571.9:c.3263G=	ENSP00000269571.4:p.Gly1088=
ENST00000406381.6:c.3173G=	ENSP00000385185.2:p.Gly1058=
ENST00000445658.6:c.2435G=	ENSP00000404047.2:p.Gly812=
ENST00000541774.5:c.3218G=	ENSP00000446466.1:p.Gly1073=
ENST00000578373.5:c.*3053G=	ENSP00000463427.1:n.*3053G=
ENST00000584450.5:c.3160-291G=	ENSP00000463714.1:n.3160-291G=
ENST00000584601.5:c.3173G=	ENSP00000462438.1:p.Gly1058=
NM_001005862.2:c.3173G= , LRG_724t1:c.3173G=	NP_001005862.1:p.Gly1058=
NM_001289936.1:c.3218G= , LRG_724t4:c.3218G=	NP_001276865.1:p.Gly1073=
NM_001289937.1:c.3160-291G=	NP_001276866.1:n.3160-291G=
NM_004448.3:c.3263G= , LRG_724t2:c.3263G=	NP_004439.2:p.Gly1088=
NR_110535.1:n.3587G=
XM_024450641.1:c.3401G=	XP_024306409.1:p.Gly1134=
XM_024450642.1:c.3356G=	XP_024306410.1:p.Gly1119=
XM_024450643.1:c.3311G=	XP_024306411.1:p.Gly1104=
NM_001005862.3:c.3173G=	NP_001005862.1:p.Gly1058=
NM_001289936.2:c.3218G=	NP_001276865.1:p.Gly1073=
NM_001289937.2:c.3160-291G=	NP_001276866.1:n.3160-291G=
NM_001382782.1:c.3173G=	NP_001369711.1:p.Gly1058=
NM_001382783.1:c.3173G=	NP_001369712.1:p.Gly1058=
NM_001382784.1:c.3380G=	NP_001369713.1:p.Gly1127=
NM_001382785.1:c.3365G=	NP_001369714.1:p.Gly1122=
NM_001382786.1:c.3344G=	NP_001369715.1:p.Gly1115=
NM_001382787.1:c.3338G=	NP_001369716.1:p.Gly1113=
NM_001382788.1:c.3293G=	NP_001369717.1:p.Gly1098=
NM_001382789.1:c.3284G=	NP_001369718.1:p.Gly1095=
NM_001382790.1:c.3260G=	NP_001369719.1:p.Gly1087=
NM_001382791.1:c.3254G=	NP_001369720.1:p.Gly1085=
NM_001382792.1:c.3227G=	NP_001369721.1:p.Gly1076=
NM_001382793.1:c.3221G=	NP_001369722.1:p.Gly1074=
NM_001382794.1:c.3221G=	NP_001369723.1:p.Gly1074=
NM_001382795.1:c.3215G=	NP_001369724.1:p.Gly1072=
NM_001382796.1:c.3176G=	NP_001369725.1:p.Gly1059=
NM_001382797.1:c.3164G=	NP_001369726.1:p.Gly1055=
NM_001382798.1:c.3107G=	NP_001369727.1:p.Gly1036=
NM_001382799.1:c.3083G=	NP_001369728.1:p.Gly1028=
NM_001382800.1:c.3077G=	NP_001369729.1:p.Gly1026=
NM_001382801.1:c.3059G=	NP_001369730.1:p.Gly1020=
NM_001382802.1:c.3005G=	NP_001369731.1:p.Gly1002=
NM_001382803.1:c.3118-291G=	NP_001369732.1:n.3118-291G=
NM_001382804.1:c.2435G=	NP_001369733.1:p.Gly812=
NM_001382805.1:c.2312G=	NP_001369734.1:p.Gly771=
NM_001382806.1:c.2225G=	NP_001369735.1:p.Gly742=
NM_004448.4:c.3263G= MANE Select	NP_004439.2:p.Gly1088=
NR_110535.2:n.3501G=