Canonical Allele Identifier: CA2259229249

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727760C= , CM000679.2:g.39727760C=	GRCh38
NC_000017.10:g.37884013C= , CM000679.1:g.37884013C=	GRCh37
NC_000017.9:g.35137539C=	NCBI36
NG_007503.1:g.44621C= , LRG_724:g.44621C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3484C= MANE Select	ENSP00000269571.4:p.Pro1162=
ENST00000269571.9:c.3484C=	ENSP00000269571.4:p.Pro1162=
ENST00000406381.6:c.3394C=	ENSP00000385185.2:p.Pro1132=
ENST00000445658.6:c.2656C=	ENSP00000404047.2:p.Pro886=
ENST00000541774.5:c.3439C=	ENSP00000446466.1:p.Pro1147=
ENST00000578373.5:c.*3274C=	ENSP00000463427.1:n.*3274C=
ENST00000584450.5:c.*63C=	ENSP00000463714.1:n.*63C=
ENST00000584601.5:c.3394C=	ENSP00000462438.1:p.Pro1132=
NM_001005862.2:c.3394C= , LRG_724t1:c.3394C=	NP_001005862.1:p.Pro1132=
NM_001289936.1:c.3439C= , LRG_724t4:c.3439C=	NP_001276865.1:p.Pro1147=
NM_001289937.1:c.*63C=	NP_001276866.1:n.*63C=
NM_004448.3:c.3484C= , LRG_724t2:c.3484C=	NP_004439.2:p.Pro1162=
NR_110535.1:n.3808C=
XM_024450641.1:c.3622C=	XP_024306409.1:p.Pro1208=
XM_024450642.1:c.3577C=	XP_024306410.1:p.Pro1193=
XM_024450643.1:c.3532C=	XP_024306411.1:p.Pro1178=
NM_001005862.3:c.3394C=	NP_001005862.1:p.Pro1132=
NM_001289936.2:c.3439C=	NP_001276865.1:p.Pro1147=
NM_001289937.2:c.*63C=	NP_001276866.1:n.*63C=
NM_001382782.1:c.3394C=	NP_001369711.1:p.Pro1132=
NM_001382783.1:c.3394C=	NP_001369712.1:p.Pro1132=
NM_001382784.1:c.3601C=	NP_001369713.1:p.Pro1201=
NM_001382785.1:c.3586C=	NP_001369714.1:p.Pro1196=
NM_001382786.1:c.3565C=	NP_001369715.1:p.Pro1189=
NM_001382787.1:c.3559C=	NP_001369716.1:p.Pro1187=
NM_001382788.1:c.3514C=	NP_001369717.1:p.Pro1172=
NM_001382789.1:c.3505C=	NP_001369718.1:p.Pro1169=
NM_001382790.1:c.3481C=	NP_001369719.1:p.Pro1161=
NM_001382791.1:c.3475C=	NP_001369720.1:p.Pro1159=
NM_001382792.1:c.3448C=	NP_001369721.1:p.Pro1150=
NM_001382793.1:c.3442C=	NP_001369722.1:p.Pro1148=
NM_001382794.1:c.3442C=	NP_001369723.1:p.Pro1148=
NM_001382795.1:c.3436C=	NP_001369724.1:p.Pro1146=
NM_001382796.1:c.3397C=	NP_001369725.1:p.Pro1133=
NM_001382797.1:c.3385C=	NP_001369726.1:p.Pro1129=
NM_001382798.1:c.3328C=	NP_001369727.1:p.Pro1110=
NM_001382799.1:c.3304C=	NP_001369728.1:p.Pro1102=
NM_001382800.1:c.3298C=	NP_001369729.1:p.Pro1100=
NM_001382801.1:c.3280C=	NP_001369730.1:p.Pro1094=
NM_001382802.1:c.3226C=	NP_001369731.1:p.Pro1076=
NM_001382803.1:c.*63C=	NP_001369732.1:n.*63C=
NM_001382804.1:c.2656C=	NP_001369733.1:p.Pro886=
NM_001382805.1:c.2533C=	NP_001369734.1:p.Pro845=
NM_001382806.1:c.2446C=	NP_001369735.1:p.Pro816=
NM_004448.4:c.3484C= MANE Select	NP_004439.2:p.Pro1162=
NR_110535.2:n.3722C=