Canonical Allele Identifier: CA2259228671

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727325G= , CM000679.2:g.39727325G=	GRCh38
NC_000017.10:g.37883578G= , CM000679.1:g.37883578G=	GRCh37
NC_000017.9:g.35137104G=	NCBI36
NG_007503.1:g.44186G= , LRG_724:g.44186G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3190G= MANE Select	ENSP00000269571.4:p.Glu1064=
ENST00000269571.9:c.3190G=	ENSP00000269571.4:p.Glu1064=
ENST00000406381.6:c.3100G=	ENSP00000385185.2:p.Glu1034=
ENST00000445658.6:c.2362G=	ENSP00000404047.2:p.Glu788=
ENST00000541774.5:c.3145G=	ENSP00000446466.1:p.Glu1049=
ENST00000578373.5:c.*2980G=	ENSP00000463427.1:n.*2980G=
ENST00000584450.5:c.3159+322G=	ENSP00000463714.1:n.3159+322G=
ENST00000584601.5:c.3100G=	ENSP00000462438.1:p.Glu1034=
NM_001005862.2:c.3100G= , LRG_724t1:c.3100G=	NP_001005862.1:p.Glu1034=
NM_001289936.1:c.3145G= , LRG_724t4:c.3145G=	NP_001276865.1:p.Glu1049=
NM_001289937.1:c.3159+322G=	NP_001276866.1:n.3159+322G=
NM_004448.3:c.3190G= , LRG_724t2:c.3190G=	NP_004439.2:p.Glu1064=
NR_110535.1:n.3514G=
XM_024450641.1:c.3328G=	XP_024306409.1:p.Glu1110=
XM_024450642.1:c.3283G=	XP_024306410.1:p.Glu1095=
XM_024450643.1:c.3238G=	XP_024306411.1:p.Glu1080=
NM_001005862.3:c.3100G=	NP_001005862.1:p.Glu1034=
NM_001289936.2:c.3145G=	NP_001276865.1:p.Glu1049=
NM_001289937.2:c.3159+322G=	NP_001276866.1:n.3159+322G=
NM_001382782.1:c.3100G=	NP_001369711.1:p.Glu1034=
NM_001382783.1:c.3100G=	NP_001369712.1:p.Glu1034=
NM_001382784.1:c.3307G=	NP_001369713.1:p.Glu1103=
NM_001382785.1:c.3292G=	NP_001369714.1:p.Glu1098=
NM_001382786.1:c.3271G=	NP_001369715.1:p.Glu1091=
NM_001382787.1:c.3265G=	NP_001369716.1:p.Glu1089=
NM_001382788.1:c.3220G=	NP_001369717.1:p.Glu1074=
NM_001382789.1:c.3211G=	NP_001369718.1:p.Glu1071=
NM_001382790.1:c.3187G=	NP_001369719.1:p.Glu1063=
NM_001382791.1:c.3181G=	NP_001369720.1:p.Glu1061=
NM_001382792.1:c.3154G=	NP_001369721.1:p.Glu1052=
NM_001382793.1:c.3148G=	NP_001369722.1:p.Glu1050=
NM_001382794.1:c.3148G=	NP_001369723.1:p.Glu1050=
NM_001382795.1:c.3142G=	NP_001369724.1:p.Glu1048=
NM_001382796.1:c.3103G=	NP_001369725.1:p.Glu1035=
NM_001382797.1:c.3091G=	NP_001369726.1:p.Glu1031=
NM_001382798.1:c.3034G=	NP_001369727.1:p.Glu1012=
NM_001382799.1:c.3010G=	NP_001369728.1:p.Glu1004=
NM_001382800.1:c.3004G=	NP_001369729.1:p.Glu1002=
NM_001382801.1:c.2986G=	NP_001369730.1:p.Glu996=
NM_001382802.1:c.2932G=	NP_001369731.1:p.Glu978=
NM_001382803.1:c.3117+322G=	NP_001369732.1:n.3117+322G=
NM_001382804.1:c.2362G=	NP_001369733.1:p.Glu788=
NM_001382805.1:c.2239G=	NP_001369734.1:p.Glu747=
NM_001382806.1:c.2152G=	NP_001369735.1:p.Glu718=
NM_004448.4:c.3190G= MANE Select	NP_004439.2:p.Glu1064=
NR_110535.2:n.3428G=