Canonical Allele Identifier: CA2259228741

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727382T= , CM000679.2:g.39727382T=	GRCh38
NC_000017.10:g.37883635T= , CM000679.1:g.37883635T=	GRCh37
NC_000017.9:g.35137161T=	NCBI36
NG_007503.1:g.44243T= , LRG_724:g.44243T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3247T= MANE Select	ENSP00000269571.4:p.Ser1083=
ENST00000269571.9:c.3247T=	ENSP00000269571.4:p.Ser1083=
ENST00000406381.6:c.3157T=	ENSP00000385185.2:p.Ser1053=
ENST00000445658.6:c.2419T=	ENSP00000404047.2:p.Ser807=
ENST00000541774.5:c.3202T=	ENSP00000446466.1:p.Ser1068=
ENST00000578373.5:c.*3037T=	ENSP00000463427.1:n.*3037T=
ENST00000584450.5:c.3160-307T=	ENSP00000463714.1:n.3160-307T=
ENST00000584601.5:c.3157T=	ENSP00000462438.1:p.Ser1053=
NM_001005862.2:c.3157T= , LRG_724t1:c.3157T=	NP_001005862.1:p.Ser1053=
NM_001289936.1:c.3202T= , LRG_724t4:c.3202T=	NP_001276865.1:p.Ser1068=
NM_001289937.1:c.3160-307T=	NP_001276866.1:n.3160-307T=
NM_004448.3:c.3247T= , LRG_724t2:c.3247T=	NP_004439.2:p.Ser1083=
NR_110535.1:n.3571T=
XM_024450641.1:c.3385T=	XP_024306409.1:p.Ser1129=
XM_024450642.1:c.3340T=	XP_024306410.1:p.Ser1114=
XM_024450643.1:c.3295T=	XP_024306411.1:p.Ser1099=
NM_001005862.3:c.3157T=	NP_001005862.1:p.Ser1053=
NM_001289936.2:c.3202T=	NP_001276865.1:p.Ser1068=
NM_001289937.2:c.3160-307T=	NP_001276866.1:n.3160-307T=
NM_001382782.1:c.3157T=	NP_001369711.1:p.Ser1053=
NM_001382783.1:c.3157T=	NP_001369712.1:p.Ser1053=
NM_001382784.1:c.3364T=	NP_001369713.1:p.Ser1122=
NM_001382785.1:c.3349T=	NP_001369714.1:p.Ser1117=
NM_001382786.1:c.3328T=	NP_001369715.1:p.Ser1110=
NM_001382787.1:c.3322T=	NP_001369716.1:p.Ser1108=
NM_001382788.1:c.3277T=	NP_001369717.1:p.Ser1093=
NM_001382789.1:c.3268T=	NP_001369718.1:p.Ser1090=
NM_001382790.1:c.3244T=	NP_001369719.1:p.Ser1082=
NM_001382791.1:c.3238T=	NP_001369720.1:p.Ser1080=
NM_001382792.1:c.3211T=	NP_001369721.1:p.Ser1071=
NM_001382793.1:c.3205T=	NP_001369722.1:p.Ser1069=
NM_001382794.1:c.3205T=	NP_001369723.1:p.Ser1069=
NM_001382795.1:c.3199T=	NP_001369724.1:p.Ser1067=
NM_001382796.1:c.3160T=	NP_001369725.1:p.Ser1054=
NM_001382797.1:c.3148T=	NP_001369726.1:p.Ser1050=
NM_001382798.1:c.3091T=	NP_001369727.1:p.Ser1031=
NM_001382799.1:c.3067T=	NP_001369728.1:p.Ser1023=
NM_001382800.1:c.3061T=	NP_001369729.1:p.Ser1021=
NM_001382801.1:c.3043T=	NP_001369730.1:p.Ser1015=
NM_001382802.1:c.2989T=	NP_001369731.1:p.Ser997=
NM_001382803.1:c.3118-307T=	NP_001369732.1:n.3118-307T=
NM_001382804.1:c.2419T=	NP_001369733.1:p.Ser807=
NM_001382805.1:c.2296T=	NP_001369734.1:p.Ser766=
NM_001382806.1:c.2209T=	NP_001369735.1:p.Ser737=
NM_004448.4:c.3247T= MANE Select	NP_004439.2:p.Ser1083=
NR_110535.2:n.3485T=