Canonical Allele Identifier: CA2259228682

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727337G= , CM000679.2:g.39727337G=	GRCh38
NC_000017.10:g.37883590G= , CM000679.1:g.37883590G=	GRCh37
NC_000017.9:g.35137116G=	NCBI36
NG_007503.1:g.44198G= , LRG_724:g.44198G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3202G= MANE Select	ENSP00000269571.4:p.Glu1068=
ENST00000269571.9:c.3202G=	ENSP00000269571.4:p.Glu1068=
ENST00000406381.6:c.3112G=	ENSP00000385185.2:p.Glu1038=
ENST00000445658.6:c.2374G=	ENSP00000404047.2:p.Glu792=
ENST00000541774.5:c.3157G=	ENSP00000446466.1:p.Glu1053=
ENST00000578373.5:c.*2992G=	ENSP00000463427.1:n.*2992G=
ENST00000584450.5:c.3159+334G=	ENSP00000463714.1:n.3159+334G=
ENST00000584601.5:c.3112G=	ENSP00000462438.1:p.Glu1038=
NM_001005862.2:c.3112G= , LRG_724t1:c.3112G=	NP_001005862.1:p.Glu1038=
NM_001289936.1:c.3157G= , LRG_724t4:c.3157G=	NP_001276865.1:p.Glu1053=
NM_001289937.1:c.3159+334G=	NP_001276866.1:n.3159+334G=
NM_004448.3:c.3202G= , LRG_724t2:c.3202G=	NP_004439.2:p.Glu1068=
NR_110535.1:n.3526G=
XM_024450641.1:c.3340G=	XP_024306409.1:p.Glu1114=
XM_024450642.1:c.3295G=	XP_024306410.1:p.Glu1099=
XM_024450643.1:c.3250G=	XP_024306411.1:p.Glu1084=
NM_001005862.3:c.3112G=	NP_001005862.1:p.Glu1038=
NM_001289936.2:c.3157G=	NP_001276865.1:p.Glu1053=
NM_001289937.2:c.3159+334G=	NP_001276866.1:n.3159+334G=
NM_001382782.1:c.3112G=	NP_001369711.1:p.Glu1038=
NM_001382783.1:c.3112G=	NP_001369712.1:p.Glu1038=
NM_001382784.1:c.3319G=	NP_001369713.1:p.Glu1107=
NM_001382785.1:c.3304G=	NP_001369714.1:p.Glu1102=
NM_001382786.1:c.3283G=	NP_001369715.1:p.Glu1095=
NM_001382787.1:c.3277G=	NP_001369716.1:p.Glu1093=
NM_001382788.1:c.3232G=	NP_001369717.1:p.Glu1078=
NM_001382789.1:c.3223G=	NP_001369718.1:p.Glu1075=
NM_001382790.1:c.3199G=	NP_001369719.1:p.Glu1067=
NM_001382791.1:c.3193G=	NP_001369720.1:p.Glu1065=
NM_001382792.1:c.3166G=	NP_001369721.1:p.Glu1056=
NM_001382793.1:c.3160G=	NP_001369722.1:p.Glu1054=
NM_001382794.1:c.3160G=	NP_001369723.1:p.Glu1054=
NM_001382795.1:c.3154G=	NP_001369724.1:p.Glu1052=
NM_001382796.1:c.3115G=	NP_001369725.1:p.Glu1039=
NM_001382797.1:c.3103G=	NP_001369726.1:p.Glu1035=
NM_001382798.1:c.3046G=	NP_001369727.1:p.Glu1016=
NM_001382799.1:c.3022G=	NP_001369728.1:p.Glu1008=
NM_001382800.1:c.3016G=	NP_001369729.1:p.Glu1006=
NM_001382801.1:c.2998G=	NP_001369730.1:p.Glu1000=
NM_001382802.1:c.2944G=	NP_001369731.1:p.Glu982=
NM_001382803.1:c.3117+334G=	NP_001369732.1:n.3117+334G=
NM_001382804.1:c.2374G=	NP_001369733.1:p.Glu792=
NM_001382805.1:c.2251G=	NP_001369734.1:p.Glu751=
NM_001382806.1:c.2164G=	NP_001369735.1:p.Glu722=
NM_004448.4:c.3202G= MANE Select	NP_004439.2:p.Glu1068=
NR_110535.2:n.3440G=