Canonical Allele Identifier: CA2259229251

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727763G= , CM000679.2:g.39727763G=	GRCh38
NC_000017.10:g.37884016G= , CM000679.1:g.37884016G=	GRCh37
NC_000017.9:g.35137542G=	NCBI36
NG_007503.1:g.44624G= , LRG_724:g.44624G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3487G= MANE Select	ENSP00000269571.4:p.Ala1163=
ENST00000269571.9:c.3487G=	ENSP00000269571.4:p.Ala1163=
ENST00000406381.6:c.3397G=	ENSP00000385185.2:p.Ala1133=
ENST00000445658.6:c.2659G=	ENSP00000404047.2:p.Ala887=
ENST00000541774.5:c.3442G=	ENSP00000446466.1:p.Ala1148=
ENST00000578373.5:c.*3277G=	ENSP00000463427.1:n.*3277G=
ENST00000584450.5:c.*66G=	ENSP00000463714.1:n.*66G=
ENST00000584601.5:c.3397G=	ENSP00000462438.1:p.Ala1133=
NM_001005862.2:c.3397G= , LRG_724t1:c.3397G=	NP_001005862.1:p.Ala1133=
NM_001289936.1:c.3442G= , LRG_724t4:c.3442G=	NP_001276865.1:p.Ala1148=
NM_001289937.1:c.*66G=	NP_001276866.1:n.*66G=
NM_004448.3:c.3487G= , LRG_724t2:c.3487G=	NP_004439.2:p.Ala1163=
NR_110535.1:n.3811G=
XM_024450641.1:c.3625G=	XP_024306409.1:p.Ala1209=
XM_024450642.1:c.3580G=	XP_024306410.1:p.Ala1194=
XM_024450643.1:c.3535G=	XP_024306411.1:p.Ala1179=
NM_001005862.3:c.3397G=	NP_001005862.1:p.Ala1133=
NM_001289936.2:c.3442G=	NP_001276865.1:p.Ala1148=
NM_001289937.2:c.*66G=	NP_001276866.1:n.*66G=
NM_001382782.1:c.3397G=	NP_001369711.1:p.Ala1133=
NM_001382783.1:c.3397G=	NP_001369712.1:p.Ala1133=
NM_001382784.1:c.3604G=	NP_001369713.1:p.Ala1202=
NM_001382785.1:c.3589G=	NP_001369714.1:p.Ala1197=
NM_001382786.1:c.3568G=	NP_001369715.1:p.Ala1190=
NM_001382787.1:c.3562G=	NP_001369716.1:p.Ala1188=
NM_001382788.1:c.3517G=	NP_001369717.1:p.Ala1173=
NM_001382789.1:c.3508G=	NP_001369718.1:p.Ala1170=
NM_001382790.1:c.3484G=	NP_001369719.1:p.Ala1162=
NM_001382791.1:c.3478G=	NP_001369720.1:p.Ala1160=
NM_001382792.1:c.3451G=	NP_001369721.1:p.Ala1151=
NM_001382793.1:c.3445G=	NP_001369722.1:p.Ala1149=
NM_001382794.1:c.3445G=	NP_001369723.1:p.Ala1149=
NM_001382795.1:c.3439G=	NP_001369724.1:p.Ala1147=
NM_001382796.1:c.3400G=	NP_001369725.1:p.Ala1134=
NM_001382797.1:c.3388G=	NP_001369726.1:p.Ala1130=
NM_001382798.1:c.3331G=	NP_001369727.1:p.Ala1111=
NM_001382799.1:c.3307G=	NP_001369728.1:p.Ala1103=
NM_001382800.1:c.3301G=	NP_001369729.1:p.Ala1101=
NM_001382801.1:c.3283G=	NP_001369730.1:p.Ala1095=
NM_001382802.1:c.3229G=	NP_001369731.1:p.Ala1077=
NM_001382803.1:c.*66G=	NP_001369732.1:n.*66G=
NM_001382804.1:c.2659G=	NP_001369733.1:p.Ala887=
NM_001382805.1:c.2536G=	NP_001369734.1:p.Ala846=
NM_001382806.1:c.2449G=	NP_001369735.1:p.Ala817=
NM_004448.4:c.3487G= MANE Select	NP_004439.2:p.Ala1163=
NR_110535.2:n.3725G=