Canonical Allele Identifier: CA2259228391
Community Standard Title: NM_004448.4(ERBB2):c.2740G= (p.Glu914=)
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39725721G= , CM000679.2:g.39725721G= GRCh38
NC_000017.10:g.37881974G= , CM000679.1:g.37881974G= GRCh37
NC_000017.9:g.35135500G= NCBI36
NG_007503.1:g.42582G= , LRG_724:g.42582G=

Transcript Alleles

HGVS Amino-acid Change
NM_004448.4:c.2740G= MANE Select NP_004439.2:p.Glu914=
ENST00000269571.10:c.2740G= MANE Select ENSP00000269571.4:p.Glu914=
NM_001005862.2:c.2650G= , LRG_724t1:c.2650G= NP_001005862.1:p.Glu884=
NM_001005862.3:c.2650G= NP_001005862.1:p.Glu884=
NM_001289936.1:c.2695G= , LRG_724t4:c.2695G= NP_001276865.1:p.Glu899=
NM_001289936.2:c.2695G= NP_001276865.1:p.Glu899=
NM_001289937.1:c.2740G= NP_001276866.1:p.Glu914=
NM_001289937.2:c.2740G= NP_001276866.1:p.Glu914=
NM_001382782.1:c.2650G= NP_001369711.1:p.Glu884=
NM_001382783.1:c.2650G= NP_001369712.1:p.Glu884=
NM_001382784.1:c.2857G= NP_001369713.1:p.Glu953=
NM_001382785.1:c.2842G= NP_001369714.1:p.Glu948=
NM_001382786.1:c.2821G= NP_001369715.1:p.Glu941=
NM_001382787.1:c.2815G= NP_001369716.1:p.Glu939=
NM_001382788.1:c.2770G= NP_001369717.1:p.Glu924=
NM_001382789.1:c.2761G= NP_001369718.1:p.Glu921=
NM_001382790.1:c.2737G= NP_001369719.1:p.Glu913=
NM_001382791.1:c.2731G= NP_001369720.1:p.Glu911=
NM_001382792.1:c.2704G= NP_001369721.1:p.Glu902=
NM_001382793.1:c.2698G= NP_001369722.1:p.Glu900=
NM_001382794.1:c.2698G= NP_001369723.1:p.Glu900=
NM_001382795.1:c.2692G= NP_001369724.1:p.Glu898=
NM_001382796.1:c.2740G= NP_001369725.1:p.Glu914=
NM_001382797.1:c.2641G= NP_001369726.1:p.Glu881=
NM_001382798.1:c.2584G= NP_001369727.1:p.Glu862=
NM_001382799.1:c.2560G= NP_001369728.1:p.Glu854=
NM_001382800.1:c.2554G= NP_001369729.1:p.Glu852=
NM_001382801.1:c.2536G= NP_001369730.1:p.Glu846=
NM_001382802.1:c.2482G= NP_001369731.1:p.Glu828=
NM_001382803.1:c.2698G= NP_001369732.1:p.Glu900=
NM_001382804.1:c.1912G= NP_001369733.1:p.Glu638=
NM_001382805.1:c.2209-1574G= NP_001369734.1:n.2209-1574G=
NM_001382806.1:c.1702G= NP_001369735.1:p.Glu568=
NM_004448.3:c.2740G= , LRG_724t2:c.2740G= NP_004439.2:p.Glu914=
NR_110535.1:n.3064G=
NR_110535.2:n.2978G=
ENST00000269571.9:c.2740G= ENSP00000269571.4:p.Glu914=
ENST00000406381.6:c.2650G= ENSP00000385185.2:p.Glu884=
ENST00000445658.6:c.1912G= ENSP00000404047.2:p.Glu638=
ENST00000541774.5:c.2695G= ENSP00000446466.1:p.Glu899=
ENST00000578373.5:c.*2530G= ENSP00000463427.1:n.*2530G=
ENST00000583038.5:n.4300G=
ENST00000584450.5:c.2740G= ENSP00000463714.1:p.Glu914=
ENST00000584601.5:c.2650G= ENSP00000462438.1:p.Glu884=
XM_024450641.1:c.2878G= XP_024306409.1:p.Glu960=
XM_024450642.1:c.2833G= XP_024306410.1:p.Glu945=
XM_024450643.1:c.2788G= XP_024306411.1:p.Glu930=