Canonical Allele Identifier: CA2259228836

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727484A= , CM000679.2:g.39727484A=	GRCh38
NC_000017.10:g.37883737A= , CM000679.1:g.37883737A=	GRCh37
NC_000017.9:g.35137263A=	NCBI36
NG_007503.1:g.44345A= , LRG_724:g.44345A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3349A= MANE Select	ENSP00000269571.4:p.Thr1117=
ENST00000269571.9:c.3349A=	ENSP00000269571.4:p.Thr1117=
ENST00000406381.6:c.3259A=	ENSP00000385185.2:p.Thr1087=
ENST00000445658.6:c.2521A=	ENSP00000404047.2:p.Thr841=
ENST00000541774.5:c.3304A=	ENSP00000446466.1:p.Thr1102=
ENST00000578373.5:c.*3139A=	ENSP00000463427.1:n.*3139A=
ENST00000584450.5:c.3160-205A=	ENSP00000463714.1:n.3160-205A=
ENST00000584601.5:c.3259A=	ENSP00000462438.1:p.Thr1087=
NM_001005862.2:c.3259A= , LRG_724t1:c.3259A=	NP_001005862.1:p.Thr1087=
NM_001289936.1:c.3304A= , LRG_724t4:c.3304A=	NP_001276865.1:p.Thr1102=
NM_001289937.1:c.3160-205A=	NP_001276866.1:n.3160-205A=
NM_004448.3:c.3349A= , LRG_724t2:c.3349A=	NP_004439.2:p.Thr1117=
NR_110535.1:n.3673A=
XM_024450641.1:c.3487A=	XP_024306409.1:p.Thr1163=
XM_024450642.1:c.3442A=	XP_024306410.1:p.Thr1148=
XM_024450643.1:c.3397A=	XP_024306411.1:p.Thr1133=
NM_001005862.3:c.3259A=	NP_001005862.1:p.Thr1087=
NM_001289936.2:c.3304A=	NP_001276865.1:p.Thr1102=
NM_001289937.2:c.3160-205A=	NP_001276866.1:n.3160-205A=
NM_001382782.1:c.3259A=	NP_001369711.1:p.Thr1087=
NM_001382783.1:c.3259A=	NP_001369712.1:p.Thr1087=
NM_001382784.1:c.3466A=	NP_001369713.1:p.Thr1156=
NM_001382785.1:c.3451A=	NP_001369714.1:p.Thr1151=
NM_001382786.1:c.3430A=	NP_001369715.1:p.Thr1144=
NM_001382787.1:c.3424A=	NP_001369716.1:p.Thr1142=
NM_001382788.1:c.3379A=	NP_001369717.1:p.Thr1127=
NM_001382789.1:c.3370A=	NP_001369718.1:p.Thr1124=
NM_001382790.1:c.3346A=	NP_001369719.1:p.Thr1116=
NM_001382791.1:c.3340A=	NP_001369720.1:p.Thr1114=
NM_001382792.1:c.3313A=	NP_001369721.1:p.Thr1105=
NM_001382793.1:c.3307A=	NP_001369722.1:p.Thr1103=
NM_001382794.1:c.3307A=	NP_001369723.1:p.Thr1103=
NM_001382795.1:c.3301A=	NP_001369724.1:p.Thr1101=
NM_001382796.1:c.3262A=	NP_001369725.1:p.Thr1088=
NM_001382797.1:c.3250A=	NP_001369726.1:p.Thr1084=
NM_001382798.1:c.3193A=	NP_001369727.1:p.Thr1065=
NM_001382799.1:c.3169A=	NP_001369728.1:p.Thr1057=
NM_001382800.1:c.3163A=	NP_001369729.1:p.Thr1055=
NM_001382801.1:c.3145A=	NP_001369730.1:p.Thr1049=
NM_001382802.1:c.3091A=	NP_001369731.1:p.Thr1031=
NM_001382803.1:c.3118-205A=	NP_001369732.1:n.3118-205A=
NM_001382804.1:c.2521A=	NP_001369733.1:p.Thr841=
NM_001382805.1:c.2398A=	NP_001369734.1:p.Thr800=
NM_001382806.1:c.2311A=	NP_001369735.1:p.Thr771=
NM_004448.4:c.3349A= MANE Select	NP_004439.2:p.Thr1117=
NR_110535.2:n.3587A=