Canonical Allele Identifier: CA2259229262

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727793C= , CM000679.2:g.39727793C=	GRCh38
NC_000017.10:g.37884046C= , CM000679.1:g.37884046C=	GRCh37
NC_000017.9:g.35137572C=	NCBI36
NG_007503.1:g.44654C= , LRG_724:g.44654C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3517C= MANE Select	ENSP00000269571.4:p.Leu1173=
ENST00000269571.9:c.3517C=	ENSP00000269571.4:p.Leu1173=
ENST00000406381.6:c.3427C=	ENSP00000385185.2:p.Leu1143=
ENST00000445658.6:c.2689C=	ENSP00000404047.2:p.Leu897=
ENST00000541774.5:c.3472C=	ENSP00000446466.1:p.Leu1158=
ENST00000578373.5:c.*3307C=	ENSP00000463427.1:n.*3307C=
ENST00000584450.5:c.*96C=	ENSP00000463714.1:n.*96C=
ENST00000584601.5:c.3427C=	ENSP00000462438.1:p.Leu1143=
NM_001005862.2:c.3427C= , LRG_724t1:c.3427C=	NP_001005862.1:p.Leu1143=
NM_001289936.1:c.3472C= , LRG_724t4:c.3472C=	NP_001276865.1:p.Leu1158=
NM_001289937.1:c.*96C=	NP_001276866.1:n.*96C=
NM_004448.3:c.3517C= , LRG_724t2:c.3517C=	NP_004439.2:p.Leu1173=
NR_110535.1:n.3841C=
XM_024450641.1:c.3655C=	XP_024306409.1:p.Leu1219=
XM_024450642.1:c.3610C=	XP_024306410.1:p.Leu1204=
XM_024450643.1:c.3565C=	XP_024306411.1:p.Leu1189=
NM_001005862.3:c.3427C=	NP_001005862.1:p.Leu1143=
NM_001289936.2:c.3472C=	NP_001276865.1:p.Leu1158=
NM_001289937.2:c.*96C=	NP_001276866.1:n.*96C=
NM_001382782.1:c.3427C=	NP_001369711.1:p.Leu1143=
NM_001382783.1:c.3427C=	NP_001369712.1:p.Leu1143=
NM_001382784.1:c.3634C=	NP_001369713.1:p.Leu1212=
NM_001382785.1:c.3619C=	NP_001369714.1:p.Leu1207=
NM_001382786.1:c.3598C=	NP_001369715.1:p.Leu1200=
NM_001382787.1:c.3592C=	NP_001369716.1:p.Leu1198=
NM_001382788.1:c.3547C=	NP_001369717.1:p.Leu1183=
NM_001382789.1:c.3538C=	NP_001369718.1:p.Leu1180=
NM_001382790.1:c.3514C=	NP_001369719.1:p.Leu1172=
NM_001382791.1:c.3508C=	NP_001369720.1:p.Leu1170=
NM_001382792.1:c.3481C=	NP_001369721.1:p.Leu1161=
NM_001382793.1:c.3475C=	NP_001369722.1:p.Leu1159=
NM_001382794.1:c.3475C=	NP_001369723.1:p.Leu1159=
NM_001382795.1:c.3469C=	NP_001369724.1:p.Leu1157=
NM_001382796.1:c.3430C=	NP_001369725.1:p.Leu1144=
NM_001382797.1:c.3418C=	NP_001369726.1:p.Leu1140=
NM_001382798.1:c.3361C=	NP_001369727.1:p.Leu1121=
NM_001382799.1:c.3337C=	NP_001369728.1:p.Leu1113=
NM_001382800.1:c.3331C=	NP_001369729.1:p.Leu1111=
NM_001382801.1:c.3313C=	NP_001369730.1:p.Leu1105=
NM_001382802.1:c.3259C=	NP_001369731.1:p.Leu1087=
NM_001382803.1:c.*96C=	NP_001369732.1:n.*96C=
NM_001382804.1:c.2689C=	NP_001369733.1:p.Leu897=
NM_001382805.1:c.2566C=	NP_001369734.1:p.Leu856=
NM_001382806.1:c.2479C=	NP_001369735.1:p.Leu827=
NM_004448.4:c.3517C= MANE Select	NP_004439.2:p.Leu1173=
NR_110535.2:n.3755C=