Canonical Allele Identifier: CA2259228784

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727411G= , CM000679.2:g.39727411G=	GRCh38
NC_000017.10:g.37883664G= , CM000679.1:g.37883664G=	GRCh37
NC_000017.9:g.35137190G=	NCBI36
NG_007503.1:g.44272G= , LRG_724:g.44272G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3276G= MANE Select	ENSP00000269571.4:p.Met1092=
ENST00000269571.9:c.3276G=	ENSP00000269571.4:p.Met1092=
ENST00000406381.6:c.3186G=	ENSP00000385185.2:p.Met1062=
ENST00000445658.6:c.2448G=	ENSP00000404047.2:p.Met816=
ENST00000541774.5:c.3231G=	ENSP00000446466.1:p.Met1077=
ENST00000578373.5:c.*3066G=	ENSP00000463427.1:n.*3066G=
ENST00000584450.5:c.3160-278G=	ENSP00000463714.1:n.3160-278G=
ENST00000584601.5:c.3186G=	ENSP00000462438.1:p.Met1062=
NM_001005862.2:c.3186G= , LRG_724t1:c.3186G=	NP_001005862.1:p.Met1062=
NM_001289936.1:c.3231G= , LRG_724t4:c.3231G=	NP_001276865.1:p.Met1077=
NM_001289937.1:c.3160-278G=	NP_001276866.1:n.3160-278G=
NM_004448.3:c.3276G= , LRG_724t2:c.3276G=	NP_004439.2:p.Met1092=
NR_110535.1:n.3600G=
XM_024450641.1:c.3414G=	XP_024306409.1:p.Met1138=
XM_024450642.1:c.3369G=	XP_024306410.1:p.Met1123=
XM_024450643.1:c.3324G=	XP_024306411.1:p.Met1108=
NM_001005862.3:c.3186G=	NP_001005862.1:p.Met1062=
NM_001289936.2:c.3231G=	NP_001276865.1:p.Met1077=
NM_001289937.2:c.3160-278G=	NP_001276866.1:n.3160-278G=
NM_001382782.1:c.3186G=	NP_001369711.1:p.Met1062=
NM_001382783.1:c.3186G=	NP_001369712.1:p.Met1062=
NM_001382784.1:c.3393G=	NP_001369713.1:p.Met1131=
NM_001382785.1:c.3378G=	NP_001369714.1:p.Met1126=
NM_001382786.1:c.3357G=	NP_001369715.1:p.Met1119=
NM_001382787.1:c.3351G=	NP_001369716.1:p.Met1117=
NM_001382788.1:c.3306G=	NP_001369717.1:p.Met1102=
NM_001382789.1:c.3297G=	NP_001369718.1:p.Met1099=
NM_001382790.1:c.3273G=	NP_001369719.1:p.Met1091=
NM_001382791.1:c.3267G=	NP_001369720.1:p.Met1089=
NM_001382792.1:c.3240G=	NP_001369721.1:p.Met1080=
NM_001382793.1:c.3234G=	NP_001369722.1:p.Met1078=
NM_001382794.1:c.3234G=	NP_001369723.1:p.Met1078=
NM_001382795.1:c.3228G=	NP_001369724.1:p.Met1076=
NM_001382796.1:c.3189G=	NP_001369725.1:p.Met1063=
NM_001382797.1:c.3177G=	NP_001369726.1:p.Met1059=
NM_001382798.1:c.3120G=	NP_001369727.1:p.Met1040=
NM_001382799.1:c.3096G=	NP_001369728.1:p.Met1032=
NM_001382800.1:c.3090G=	NP_001369729.1:p.Met1030=
NM_001382801.1:c.3072G=	NP_001369730.1:p.Met1024=
NM_001382802.1:c.3018G=	NP_001369731.1:p.Met1006=
NM_001382803.1:c.3118-278G=	NP_001369732.1:n.3118-278G=
NM_001382804.1:c.2448G=	NP_001369733.1:p.Met816=
NM_001382805.1:c.2325G=	NP_001369734.1:p.Met775=
NM_001382806.1:c.2238G=	NP_001369735.1:p.Met746=
NM_004448.4:c.3276G= MANE Select	NP_004439.2:p.Met1092=
NR_110535.2:n.3514G=