Canonical Allele Identifier: CA2259228827

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727473G= , CM000679.2:g.39727473G=	GRCh38
NC_000017.10:g.37883726G= , CM000679.1:g.37883726G=	GRCh37
NC_000017.9:g.35137252G=	NCBI36
NG_007503.1:g.44334G= , LRG_724:g.44334G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3338G= MANE Select	ENSP00000269571.4:p.Ser1113=
ENST00000269571.9:c.3338G=	ENSP00000269571.4:p.Ser1113=
ENST00000406381.6:c.3248G=	ENSP00000385185.2:p.Ser1083=
ENST00000445658.6:c.2510G=	ENSP00000404047.2:p.Ser837=
ENST00000541774.5:c.3293G=	ENSP00000446466.1:p.Ser1098=
ENST00000578373.5:c.*3128G=	ENSP00000463427.1:n.*3128G=
ENST00000584450.5:c.3160-216G=	ENSP00000463714.1:n.3160-216G=
ENST00000584601.5:c.3248G=	ENSP00000462438.1:p.Ser1083=
NM_001005862.2:c.3248G= , LRG_724t1:c.3248G=	NP_001005862.1:p.Ser1083=
NM_001289936.1:c.3293G= , LRG_724t4:c.3293G=	NP_001276865.1:p.Ser1098=
NM_001289937.1:c.3160-216G=	NP_001276866.1:n.3160-216G=
NM_004448.3:c.3338G= , LRG_724t2:c.3338G=	NP_004439.2:p.Ser1113=
NR_110535.1:n.3662G=
XM_024450641.1:c.3476G=	XP_024306409.1:p.Ser1159=
XM_024450642.1:c.3431G=	XP_024306410.1:p.Ser1144=
XM_024450643.1:c.3386G=	XP_024306411.1:p.Ser1129=
NM_001005862.3:c.3248G=	NP_001005862.1:p.Ser1083=
NM_001289936.2:c.3293G=	NP_001276865.1:p.Ser1098=
NM_001289937.2:c.3160-216G=	NP_001276866.1:n.3160-216G=
NM_001382782.1:c.3248G=	NP_001369711.1:p.Ser1083=
NM_001382783.1:c.3248G=	NP_001369712.1:p.Ser1083=
NM_001382784.1:c.3455G=	NP_001369713.1:p.Ser1152=
NM_001382785.1:c.3440G=	NP_001369714.1:p.Ser1147=
NM_001382786.1:c.3419G=	NP_001369715.1:p.Ser1140=
NM_001382787.1:c.3413G=	NP_001369716.1:p.Ser1138=
NM_001382788.1:c.3368G=	NP_001369717.1:p.Ser1123=
NM_001382789.1:c.3359G=	NP_001369718.1:p.Ser1120=
NM_001382790.1:c.3335G=	NP_001369719.1:p.Ser1112=
NM_001382791.1:c.3329G=	NP_001369720.1:p.Ser1110=
NM_001382792.1:c.3302G=	NP_001369721.1:p.Ser1101=
NM_001382793.1:c.3296G=	NP_001369722.1:p.Ser1099=
NM_001382794.1:c.3296G=	NP_001369723.1:p.Ser1099=
NM_001382795.1:c.3290G=	NP_001369724.1:p.Ser1097=
NM_001382796.1:c.3251G=	NP_001369725.1:p.Ser1084=
NM_001382797.1:c.3239G=	NP_001369726.1:p.Ser1080=
NM_001382798.1:c.3182G=	NP_001369727.1:p.Ser1061=
NM_001382799.1:c.3158G=	NP_001369728.1:p.Ser1053=
NM_001382800.1:c.3152G=	NP_001369729.1:p.Ser1051=
NM_001382801.1:c.3134G=	NP_001369730.1:p.Ser1045=
NM_001382802.1:c.3080G=	NP_001369731.1:p.Ser1027=
NM_001382803.1:c.3118-216G=	NP_001369732.1:n.3118-216G=
NM_001382804.1:c.2510G=	NP_001369733.1:p.Ser837=
NM_001382805.1:c.2387G=	NP_001369734.1:p.Ser796=
NM_001382806.1:c.2300G=	NP_001369735.1:p.Ser767=
NM_004448.4:c.3338G= MANE Select	NP_004439.2:p.Ser1113=
NR_110535.2:n.3576G=