Canonical Allele Identifier: CA2259229293

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727850G= , CM000679.2:g.39727850G=	GRCh38
NC_000017.10:g.37884103G= , CM000679.1:g.37884103G=	GRCh37
NC_000017.9:g.35137629G=	NCBI36
NG_007503.1:g.44711G= , LRG_724:g.44711G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3574G= MANE Select	ENSP00000269571.4:p.Glu1192=
ENST00000269571.9:c.3574G=	ENSP00000269571.4:p.Glu1192=
ENST00000406381.6:c.3484G=	ENSP00000385185.2:p.Glu1162=
ENST00000445658.6:c.2746G=	ENSP00000404047.2:p.Glu916=
ENST00000541774.5:c.3529G=	ENSP00000446466.1:p.Glu1177=
ENST00000578373.5:c.*3364G=	ENSP00000463427.1:n.*3364G=
ENST00000584450.5:c.*153G=	ENSP00000463714.1:n.*153G=
ENST00000584601.5:c.3484G=	ENSP00000462438.1:p.Glu1162=
NM_001005862.2:c.3484G= , LRG_724t1:c.3484G=	NP_001005862.1:p.Glu1162=
NM_001289936.1:c.3529G= , LRG_724t4:c.3529G=	NP_001276865.1:p.Glu1177=
NM_001289937.1:c.*153G=	NP_001276866.1:n.*153G=
NM_004448.3:c.3574G= , LRG_724t2:c.3574G=	NP_004439.2:p.Glu1192=
NR_110535.1:n.3898G=
XM_024450641.1:c.3712G=	XP_024306409.1:p.Glu1238=
XM_024450642.1:c.3667G=	XP_024306410.1:p.Glu1223=
XM_024450643.1:c.3622G=	XP_024306411.1:p.Glu1208=
NM_001005862.3:c.3484G=	NP_001005862.1:p.Glu1162=
NM_001289936.2:c.3529G=	NP_001276865.1:p.Glu1177=
NM_001289937.2:c.*153G=	NP_001276866.1:n.*153G=
NM_001382782.1:c.3484G=	NP_001369711.1:p.Glu1162=
NM_001382783.1:c.3484G=	NP_001369712.1:p.Glu1162=
NM_001382784.1:c.3691G=	NP_001369713.1:p.Glu1231=
NM_001382785.1:c.3676G=	NP_001369714.1:p.Glu1226=
NM_001382786.1:c.3655G=	NP_001369715.1:p.Glu1219=
NM_001382787.1:c.3649G=	NP_001369716.1:p.Glu1217=
NM_001382788.1:c.3604G=	NP_001369717.1:p.Glu1202=
NM_001382789.1:c.3595G=	NP_001369718.1:p.Glu1199=
NM_001382790.1:c.3571G=	NP_001369719.1:p.Glu1191=
NM_001382791.1:c.3565G=	NP_001369720.1:p.Glu1189=
NM_001382792.1:c.3538G=	NP_001369721.1:p.Glu1180=
NM_001382793.1:c.3532G=	NP_001369722.1:p.Glu1178=
NM_001382794.1:c.3532G=	NP_001369723.1:p.Glu1178=
NM_001382795.1:c.3526G=	NP_001369724.1:p.Glu1176=
NM_001382796.1:c.3487G=	NP_001369725.1:p.Glu1163=
NM_001382797.1:c.3475G=	NP_001369726.1:p.Glu1159=
NM_001382798.1:c.3418G=	NP_001369727.1:p.Glu1140=
NM_001382799.1:c.3394G=	NP_001369728.1:p.Glu1132=
NM_001382800.1:c.3388G=	NP_001369729.1:p.Glu1130=
NM_001382801.1:c.3370G=	NP_001369730.1:p.Glu1124=
NM_001382802.1:c.3316G=	NP_001369731.1:p.Glu1106=
NM_001382803.1:c.*153G=	NP_001369732.1:n.*153G=
NM_001382804.1:c.2746G=	NP_001369733.1:p.Glu916=
NM_001382805.1:c.2623G=	NP_001369734.1:p.Glu875=
NM_001382806.1:c.2536G=	NP_001369735.1:p.Glu846=
NM_004448.4:c.3574G= MANE Select	NP_004439.2:p.Glu1192=
NR_110535.2:n.3812G=