Canonical Allele Identifier: CA2259229336

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727969G= , CM000679.2:g.39727969G=	GRCh38
NC_000017.10:g.37884222G= , CM000679.1:g.37884222G=	GRCh37
NC_000017.9:g.35137748G=	NCBI36
NG_007503.1:g.44830G= , LRG_724:g.44830G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3693G= MANE Select	ENSP00000269571.4:p.Gly1231=
ENST00000269571.9:c.3693G=	ENSP00000269571.4:p.Gly1231=
ENST00000406381.6:c.3603G=	ENSP00000385185.2:p.Gly1201=
ENST00000445658.6:c.2865G=	ENSP00000404047.2:p.Gly955=
ENST00000541774.5:c.3648G=	ENSP00000446466.1:p.Gly1216=
ENST00000578373.5:c.*3483G=	ENSP00000463427.1:n.*3483G=
ENST00000584450.5:c.*272G=	ENSP00000463714.1:n.*272G=
ENST00000584601.5:c.3603G=	ENSP00000462438.1:p.Gly1201=
NM_001005862.2:c.3603G= , LRG_724t1:c.3603G=	NP_001005862.1:p.Gly1201=
NM_001289936.1:c.3648G= , LRG_724t4:c.3648G=	NP_001276865.1:p.Gly1216=
NM_001289937.1:c.*272G=	NP_001276866.1:n.*272G=
NM_004448.3:c.3693G= , LRG_724t2:c.3693G=	NP_004439.2:p.Gly1231=
NR_110535.1:n.4017G=
XM_024450641.1:c.3831G=	XP_024306409.1:p.Gly1277=
XM_024450642.1:c.3786G=	XP_024306410.1:p.Gly1262=
XM_024450643.1:c.3741G=	XP_024306411.1:p.Gly1247=
NM_001005862.3:c.3603G=	NP_001005862.1:p.Gly1201=
NM_001289936.2:c.3648G=	NP_001276865.1:p.Gly1216=
NM_001289937.2:c.*272G=	NP_001276866.1:n.*272G=
NM_001382782.1:c.3603G=	NP_001369711.1:p.Gly1201=
NM_001382783.1:c.3603G=	NP_001369712.1:p.Gly1201=
NM_001382784.1:c.3810G=	NP_001369713.1:p.Gly1270=
NM_001382785.1:c.3795G=	NP_001369714.1:p.Gly1265=
NM_001382786.1:c.3774G=	NP_001369715.1:p.Gly1258=
NM_001382787.1:c.3768G=	NP_001369716.1:p.Gly1256=
NM_001382788.1:c.3723G=	NP_001369717.1:p.Gly1241=
NM_001382789.1:c.3714G=	NP_001369718.1:p.Gly1238=
NM_001382790.1:c.3690G=	NP_001369719.1:p.Gly1230=
NM_001382791.1:c.3684G=	NP_001369720.1:p.Gly1228=
NM_001382792.1:c.3657G=	NP_001369721.1:p.Gly1219=
NM_001382793.1:c.3651G=	NP_001369722.1:p.Gly1217=
NM_001382794.1:c.3651G=	NP_001369723.1:p.Gly1217=
NM_001382795.1:c.3645G=	NP_001369724.1:p.Gly1215=
NM_001382796.1:c.3606G=	NP_001369725.1:p.Gly1202=
NM_001382797.1:c.3594G=	NP_001369726.1:p.Gly1198=
NM_001382798.1:c.3537G=	NP_001369727.1:p.Gly1179=
NM_001382799.1:c.3513G=	NP_001369728.1:p.Gly1171=
NM_001382800.1:c.3507G=	NP_001369729.1:p.Gly1169=
NM_001382801.1:c.3489G=	NP_001369730.1:p.Gly1163=
NM_001382802.1:c.3435G=	NP_001369731.1:p.Gly1145=
NM_001382803.1:c.*272G=	NP_001369732.1:n.*272G=
NM_001382804.1:c.2865G=	NP_001369733.1:p.Gly955=
NM_001382805.1:c.2742G=	NP_001369734.1:p.Gly914=
NM_001382806.1:c.2655G=	NP_001369735.1:p.Gly885=
NM_004448.4:c.3693G= MANE Select	NP_004439.2:p.Gly1231=
NR_110535.2:n.3931G=