Canonical Allele Identifier: CA2259228726

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727367T= , CM000679.2:g.39727367T=	GRCh38
NC_000017.10:g.37883620T= , CM000679.1:g.37883620T=	GRCh37
NC_000017.9:g.35137146T=	NCBI36
NG_007503.1:g.44228T= , LRG_724:g.44228T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3232T= MANE Select	ENSP00000269571.4:p.Ser1078=
ENST00000269571.9:c.3232T=	ENSP00000269571.4:p.Ser1078=
ENST00000406381.6:c.3142T=	ENSP00000385185.2:p.Ser1048=
ENST00000445658.6:c.2404T=	ENSP00000404047.2:p.Ser802=
ENST00000541774.5:c.3187T=	ENSP00000446466.1:p.Ser1063=
ENST00000578373.5:c.*3022T=	ENSP00000463427.1:n.*3022T=
ENST00000584450.5:c.3160-322T=	ENSP00000463714.1:n.3160-322T=
ENST00000584601.5:c.3142T=	ENSP00000462438.1:p.Ser1048=
NM_001005862.2:c.3142T= , LRG_724t1:c.3142T=	NP_001005862.1:p.Ser1048=
NM_001289936.1:c.3187T= , LRG_724t4:c.3187T=	NP_001276865.1:p.Ser1063=
NM_001289937.1:c.3160-322T=	NP_001276866.1:n.3160-322T=
NM_004448.3:c.3232T= , LRG_724t2:c.3232T=	NP_004439.2:p.Ser1078=
NR_110535.1:n.3556T=
XM_024450641.1:c.3370T=	XP_024306409.1:p.Ser1124=
XM_024450642.1:c.3325T=	XP_024306410.1:p.Ser1109=
XM_024450643.1:c.3280T=	XP_024306411.1:p.Ser1094=
NM_001005862.3:c.3142T=	NP_001005862.1:p.Ser1048=
NM_001289936.2:c.3187T=	NP_001276865.1:p.Ser1063=
NM_001289937.2:c.3160-322T=	NP_001276866.1:n.3160-322T=
NM_001382782.1:c.3142T=	NP_001369711.1:p.Ser1048=
NM_001382783.1:c.3142T=	NP_001369712.1:p.Ser1048=
NM_001382784.1:c.3349T=	NP_001369713.1:p.Ser1117=
NM_001382785.1:c.3334T=	NP_001369714.1:p.Ser1112=
NM_001382786.1:c.3313T=	NP_001369715.1:p.Ser1105=
NM_001382787.1:c.3307T=	NP_001369716.1:p.Ser1103=
NM_001382788.1:c.3262T=	NP_001369717.1:p.Ser1088=
NM_001382789.1:c.3253T=	NP_001369718.1:p.Ser1085=
NM_001382790.1:c.3229T=	NP_001369719.1:p.Ser1077=
NM_001382791.1:c.3223T=	NP_001369720.1:p.Ser1075=
NM_001382792.1:c.3196T=	NP_001369721.1:p.Ser1066=
NM_001382793.1:c.3190T=	NP_001369722.1:p.Ser1064=
NM_001382794.1:c.3190T=	NP_001369723.1:p.Ser1064=
NM_001382795.1:c.3184T=	NP_001369724.1:p.Ser1062=
NM_001382796.1:c.3145T=	NP_001369725.1:p.Ser1049=
NM_001382797.1:c.3133T=	NP_001369726.1:p.Ser1045=
NM_001382798.1:c.3076T=	NP_001369727.1:p.Ser1026=
NM_001382799.1:c.3052T=	NP_001369728.1:p.Ser1018=
NM_001382800.1:c.3046T=	NP_001369729.1:p.Ser1016=
NM_001382801.1:c.3028T=	NP_001369730.1:p.Ser1010=
NM_001382802.1:c.2974T=	NP_001369731.1:p.Ser992=
NM_001382803.1:c.3118-322T=	NP_001369732.1:n.3118-322T=
NM_001382804.1:c.2404T=	NP_001369733.1:p.Ser802=
NM_001382805.1:c.2281T=	NP_001369734.1:p.Ser761=
NM_001382806.1:c.2194T=	NP_001369735.1:p.Ser732=
NM_004448.4:c.3232T= MANE Select	NP_004439.2:p.Ser1078=
NR_110535.2:n.3470T=