Canonical Allele Identifier: CA2259228782

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727410T= , CM000679.2:g.39727410T=	GRCh38
NC_000017.10:g.37883663T= , CM000679.1:g.37883663T=	GRCh37
NC_000017.9:g.35137189T=	NCBI36
NG_007503.1:g.44271T= , LRG_724:g.44271T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3275T= MANE Select	ENSP00000269571.4:p.Met1092=
ENST00000269571.9:c.3275T=	ENSP00000269571.4:p.Met1092=
ENST00000406381.6:c.3185T=	ENSP00000385185.2:p.Met1062=
ENST00000445658.6:c.2447T=	ENSP00000404047.2:p.Met816=
ENST00000541774.5:c.3230T=	ENSP00000446466.1:p.Met1077=
ENST00000578373.5:c.*3065T=	ENSP00000463427.1:n.*3065T=
ENST00000584450.5:c.3160-279T=	ENSP00000463714.1:n.3160-279T=
ENST00000584601.5:c.3185T=	ENSP00000462438.1:p.Met1062=
NM_001005862.2:c.3185T= , LRG_724t1:c.3185T=	NP_001005862.1:p.Met1062=
NM_001289936.1:c.3230T= , LRG_724t4:c.3230T=	NP_001276865.1:p.Met1077=
NM_001289937.1:c.3160-279T=	NP_001276866.1:n.3160-279T=
NM_004448.3:c.3275T= , LRG_724t2:c.3275T=	NP_004439.2:p.Met1092=
NR_110535.1:n.3599T=
XM_024450641.1:c.3413T=	XP_024306409.1:p.Met1138=
XM_024450642.1:c.3368T=	XP_024306410.1:p.Met1123=
XM_024450643.1:c.3323T=	XP_024306411.1:p.Met1108=
NM_001005862.3:c.3185T=	NP_001005862.1:p.Met1062=
NM_001289936.2:c.3230T=	NP_001276865.1:p.Met1077=
NM_001289937.2:c.3160-279T=	NP_001276866.1:n.3160-279T=
NM_001382782.1:c.3185T=	NP_001369711.1:p.Met1062=
NM_001382783.1:c.3185T=	NP_001369712.1:p.Met1062=
NM_001382784.1:c.3392T=	NP_001369713.1:p.Met1131=
NM_001382785.1:c.3377T=	NP_001369714.1:p.Met1126=
NM_001382786.1:c.3356T=	NP_001369715.1:p.Met1119=
NM_001382787.1:c.3350T=	NP_001369716.1:p.Met1117=
NM_001382788.1:c.3305T=	NP_001369717.1:p.Met1102=
NM_001382789.1:c.3296T=	NP_001369718.1:p.Met1099=
NM_001382790.1:c.3272T=	NP_001369719.1:p.Met1091=
NM_001382791.1:c.3266T=	NP_001369720.1:p.Met1089=
NM_001382792.1:c.3239T=	NP_001369721.1:p.Met1080=
NM_001382793.1:c.3233T=	NP_001369722.1:p.Met1078=
NM_001382794.1:c.3233T=	NP_001369723.1:p.Met1078=
NM_001382795.1:c.3227T=	NP_001369724.1:p.Met1076=
NM_001382796.1:c.3188T=	NP_001369725.1:p.Met1063=
NM_001382797.1:c.3176T=	NP_001369726.1:p.Met1059=
NM_001382798.1:c.3119T=	NP_001369727.1:p.Met1040=
NM_001382799.1:c.3095T=	NP_001369728.1:p.Met1032=
NM_001382800.1:c.3089T=	NP_001369729.1:p.Met1030=
NM_001382801.1:c.3071T=	NP_001369730.1:p.Met1024=
NM_001382802.1:c.3017T=	NP_001369731.1:p.Met1006=
NM_001382803.1:c.3118-279T=	NP_001369732.1:n.3118-279T=
NM_001382804.1:c.2447T=	NP_001369733.1:p.Met816=
NM_001382805.1:c.2324T=	NP_001369734.1:p.Met775=
NM_001382806.1:c.2237T=	NP_001369735.1:p.Met746=
NM_004448.4:c.3275T= MANE Select	NP_004439.2:p.Met1092=
NR_110535.2:n.3513T=