Canonical Allele Identifier: CA2259229295

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727856C= , CM000679.2:g.39727856C=	GRCh38
NC_000017.10:g.37884109C= , CM000679.1:g.37884109C=	GRCh37
NC_000017.9:g.35137635C=	NCBI36
NG_007503.1:g.44717C= , LRG_724:g.44717C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3580C= MANE Select	ENSP00000269571.4:p.Pro1194=
ENST00000269571.9:c.3580C=	ENSP00000269571.4:p.Pro1194=
ENST00000406381.6:c.3490C=	ENSP00000385185.2:p.Pro1164=
ENST00000445658.6:c.2752C=	ENSP00000404047.2:p.Pro918=
ENST00000541774.5:c.3535C=	ENSP00000446466.1:p.Pro1179=
ENST00000578373.5:c.*3370C=	ENSP00000463427.1:n.*3370C=
ENST00000584450.5:c.*159C=	ENSP00000463714.1:n.*159C=
ENST00000584601.5:c.3490C=	ENSP00000462438.1:p.Pro1164=
NM_001005862.2:c.3490C= , LRG_724t1:c.3490C=	NP_001005862.1:p.Pro1164=
NM_001289936.1:c.3535C= , LRG_724t4:c.3535C=	NP_001276865.1:p.Pro1179=
NM_001289937.1:c.*159C=	NP_001276866.1:n.*159C=
NM_004448.3:c.3580C= , LRG_724t2:c.3580C=	NP_004439.2:p.Pro1194=
NR_110535.1:n.3904C=
XM_024450641.1:c.3718C=	XP_024306409.1:p.Pro1240=
XM_024450642.1:c.3673C=	XP_024306410.1:p.Pro1225=
XM_024450643.1:c.3628C=	XP_024306411.1:p.Pro1210=
NM_001005862.3:c.3490C=	NP_001005862.1:p.Pro1164=
NM_001289936.2:c.3535C=	NP_001276865.1:p.Pro1179=
NM_001289937.2:c.*159C=	NP_001276866.1:n.*159C=
NM_001382782.1:c.3490C=	NP_001369711.1:p.Pro1164=
NM_001382783.1:c.3490C=	NP_001369712.1:p.Pro1164=
NM_001382784.1:c.3697C=	NP_001369713.1:p.Pro1233=
NM_001382785.1:c.3682C=	NP_001369714.1:p.Pro1228=
NM_001382786.1:c.3661C=	NP_001369715.1:p.Pro1221=
NM_001382787.1:c.3655C=	NP_001369716.1:p.Pro1219=
NM_001382788.1:c.3610C=	NP_001369717.1:p.Pro1204=
NM_001382789.1:c.3601C=	NP_001369718.1:p.Pro1201=
NM_001382790.1:c.3577C=	NP_001369719.1:p.Pro1193=
NM_001382791.1:c.3571C=	NP_001369720.1:p.Pro1191=
NM_001382792.1:c.3544C=	NP_001369721.1:p.Pro1182=
NM_001382793.1:c.3538C=	NP_001369722.1:p.Pro1180=
NM_001382794.1:c.3538C=	NP_001369723.1:p.Pro1180=
NM_001382795.1:c.3532C=	NP_001369724.1:p.Pro1178=
NM_001382796.1:c.3493C=	NP_001369725.1:p.Pro1165=
NM_001382797.1:c.3481C=	NP_001369726.1:p.Pro1161=
NM_001382798.1:c.3424C=	NP_001369727.1:p.Pro1142=
NM_001382799.1:c.3400C=	NP_001369728.1:p.Pro1134=
NM_001382800.1:c.3394C=	NP_001369729.1:p.Pro1132=
NM_001382801.1:c.3376C=	NP_001369730.1:p.Pro1126=
NM_001382802.1:c.3322C=	NP_001369731.1:p.Pro1108=
NM_001382803.1:c.*159C=	NP_001369732.1:n.*159C=
NM_001382804.1:c.2752C=	NP_001369733.1:p.Pro918=
NM_001382805.1:c.2629C=	NP_001369734.1:p.Pro877=
NM_001382806.1:c.2542C=	NP_001369735.1:p.Pro848=
NM_004448.4:c.3580C= MANE Select	NP_004439.2:p.Pro1194=
NR_110535.2:n.3818C=