Canonical Allele Identifier: CA2259229297

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727859G= , CM000679.2:g.39727859G=	GRCh38
NC_000017.10:g.37884112G= , CM000679.1:g.37884112G=	GRCh37
NC_000017.9:g.35137638G=	NCBI36
NG_007503.1:g.44720G= , LRG_724:g.44720G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3583G= MANE Select	ENSP00000269571.4:p.Glu1195=
ENST00000269571.9:c.3583G=	ENSP00000269571.4:p.Glu1195=
ENST00000406381.6:c.3493G=	ENSP00000385185.2:p.Glu1165=
ENST00000445658.6:c.2755G=	ENSP00000404047.2:p.Glu919=
ENST00000541774.5:c.3538G=	ENSP00000446466.1:p.Glu1180=
ENST00000578373.5:c.*3373G=	ENSP00000463427.1:n.*3373G=
ENST00000584450.5:c.*162G=	ENSP00000463714.1:n.*162G=
ENST00000584601.5:c.3493G=	ENSP00000462438.1:p.Glu1165=
NM_001005862.2:c.3493G= , LRG_724t1:c.3493G=	NP_001005862.1:p.Glu1165=
NM_001289936.1:c.3538G= , LRG_724t4:c.3538G=	NP_001276865.1:p.Glu1180=
NM_001289937.1:c.*162G=	NP_001276866.1:n.*162G=
NM_004448.3:c.3583G= , LRG_724t2:c.3583G=	NP_004439.2:p.Glu1195=
NR_110535.1:n.3907G=
XM_024450641.1:c.3721G=	XP_024306409.1:p.Glu1241=
XM_024450642.1:c.3676G=	XP_024306410.1:p.Glu1226=
XM_024450643.1:c.3631G=	XP_024306411.1:p.Glu1211=
NM_001005862.3:c.3493G=	NP_001005862.1:p.Glu1165=
NM_001289936.2:c.3538G=	NP_001276865.1:p.Glu1180=
NM_001289937.2:c.*162G=	NP_001276866.1:n.*162G=
NM_001382782.1:c.3493G=	NP_001369711.1:p.Glu1165=
NM_001382783.1:c.3493G=	NP_001369712.1:p.Glu1165=
NM_001382784.1:c.3700G=	NP_001369713.1:p.Glu1234=
NM_001382785.1:c.3685G=	NP_001369714.1:p.Glu1229=
NM_001382786.1:c.3664G=	NP_001369715.1:p.Glu1222=
NM_001382787.1:c.3658G=	NP_001369716.1:p.Glu1220=
NM_001382788.1:c.3613G=	NP_001369717.1:p.Glu1205=
NM_001382789.1:c.3604G=	NP_001369718.1:p.Glu1202=
NM_001382790.1:c.3580G=	NP_001369719.1:p.Glu1194=
NM_001382791.1:c.3574G=	NP_001369720.1:p.Glu1192=
NM_001382792.1:c.3547G=	NP_001369721.1:p.Glu1183=
NM_001382793.1:c.3541G=	NP_001369722.1:p.Glu1181=
NM_001382794.1:c.3541G=	NP_001369723.1:p.Glu1181=
NM_001382795.1:c.3535G=	NP_001369724.1:p.Glu1179=
NM_001382796.1:c.3496G=	NP_001369725.1:p.Glu1166=
NM_001382797.1:c.3484G=	NP_001369726.1:p.Glu1162=
NM_001382798.1:c.3427G=	NP_001369727.1:p.Glu1143=
NM_001382799.1:c.3403G=	NP_001369728.1:p.Glu1135=
NM_001382800.1:c.3397G=	NP_001369729.1:p.Glu1133=
NM_001382801.1:c.3379G=	NP_001369730.1:p.Glu1127=
NM_001382802.1:c.3325G=	NP_001369731.1:p.Glu1109=
NM_001382803.1:c.*162G=	NP_001369732.1:n.*162G=
NM_001382804.1:c.2755G=	NP_001369733.1:p.Glu919=
NM_001382805.1:c.2632G=	NP_001369734.1:p.Glu878=
NM_001382806.1:c.2545G=	NP_001369735.1:p.Glu849=
NM_004448.4:c.3583G= MANE Select	NP_004439.2:p.Glu1195=
NR_110535.2:n.3821G=