Canonical Allele Identifier: CA2259227995

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724756C= , CM000679.2:g.39724756C=	GRCh38
NC_000017.10:g.37881009C= , CM000679.1:g.37881009C=	GRCh37
NC_000017.9:g.35134535C=	NCBI36
NG_007503.1:g.41617C= , LRG_724:g.41617C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2338C= MANE Select	ENSP00000269571.4:p.Pro780=
ENST00000269571.9:c.2338C=	ENSP00000269571.4:p.Pro780=
ENST00000406381.6:c.2248C=	ENSP00000385185.2:p.Pro750=
ENST00000445658.6:c.1510C=	ENSP00000404047.2:p.Pro504=
ENST00000541774.5:c.2293C=	ENSP00000446466.1:p.Pro765=
ENST00000578373.5:c.*2128C=	ENSP00000463427.1:n.*2128C=
ENST00000580074.1:c.444C=
ENST00000583038.5:n.3472C=
ENST00000584450.5:c.2338C=	ENSP00000463714.1:p.Pro780=
ENST00000584601.5:c.2248C=	ENSP00000462438.1:p.Pro750=
NM_001005862.2:c.2248C= , LRG_724t1:c.2248C=	NP_001005862.1:p.Pro750=
NM_001289936.1:c.2293C= , LRG_724t4:c.2293C=	NP_001276865.1:p.Pro765=
NM_001289937.1:c.2338C=	NP_001276866.1:p.Pro780=
NM_004448.3:c.2338C= , LRG_724t2:c.2338C=	NP_004439.2:p.Pro780=
NR_110535.1:n.2662C=
XM_024450641.1:c.2476C=	XP_024306409.1:p.Pro826=
XM_024450642.1:c.2431C=	XP_024306410.1:p.Pro811=
XM_024450643.1:c.2386C=	XP_024306411.1:p.Pro796=
NM_001005862.3:c.2248C=	NP_001005862.1:p.Pro750=
NM_001289936.2:c.2293C=	NP_001276865.1:p.Pro765=
NM_001289937.2:c.2338C=	NP_001276866.1:p.Pro780=
NM_001382782.1:c.2248C=	NP_001369711.1:p.Pro750=
NM_001382783.1:c.2248C=	NP_001369712.1:p.Pro750=
NM_001382784.1:c.2455C=	NP_001369713.1:p.Pro819=
NM_001382785.1:c.2440C=	NP_001369714.1:p.Pro814=
NM_001382786.1:c.2419C=	NP_001369715.1:p.Pro807=
NM_001382787.1:c.2413C=	NP_001369716.1:p.Pro805=
NM_001382788.1:c.2368C=	NP_001369717.1:p.Pro790=
NM_001382789.1:c.2359C=	NP_001369718.1:p.Pro787=
NM_001382790.1:c.2335C=	NP_001369719.1:p.Pro779=
NM_001382791.1:c.2329C=	NP_001369720.1:p.Pro777=
NM_001382792.1:c.2302C=	NP_001369721.1:p.Pro768=
NM_001382793.1:c.2296C=	NP_001369722.1:p.Pro766=
NM_001382794.1:c.2296C=	NP_001369723.1:p.Pro766=
NM_001382795.1:c.2290C=	NP_001369724.1:p.Pro764=
NM_001382796.1:c.2338C=	NP_001369725.1:p.Pro780=
NM_001382797.1:c.2239C=	NP_001369726.1:p.Pro747=
NM_001382798.1:c.2338C=	NP_001369727.1:p.Pro780=
NM_001382799.1:c.2158C=	NP_001369728.1:p.Pro720=
NM_001382800.1:c.2308-293C=	NP_001369729.1:n.2308-293C=
NM_001382801.1:c.2290C=	NP_001369730.1:p.Pro764=
NM_001382802.1:c.2080C=	NP_001369731.1:p.Pro694=
NM_001382803.1:c.2296C=	NP_001369732.1:p.Pro766=
NM_001382804.1:c.1510C=	NP_001369733.1:p.Pro504=
NM_001382805.1:c.2208+1096C=	NP_001369734.1:n.2208+1096C=
NM_001382806.1:c.1300C=	NP_001369735.1:p.Pro434=
NM_004448.4:c.2338C= MANE Select	NP_004439.2:p.Pro780=
NR_110535.2:n.2576C=