Canonical Allele Identifier: CA2259229137
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727502G= , CM000679.2:g.39727502G= GRCh38
NC_000017.10:g.37883755G= , CM000679.1:g.37883755G= GRCh37
NC_000017.9:g.35137281G= NCBI36
NG_007503.1:g.44363G= , LRG_724:g.44363G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3367G= MANE Select ENSP00000269571.4:p.Glu1123=
ENST00000269571.9:c.3367G= ENSP00000269571.4:p.Glu1123=
ENST00000406381.6:c.3277G= ENSP00000385185.2:p.Glu1093=
ENST00000445658.6:c.2539G= ENSP00000404047.2:p.Glu847=
ENST00000541774.5:c.3322G= ENSP00000446466.1:p.Glu1108=
ENST00000578373.5:c.*3157G= ENSP00000463427.1:n.*3157G=
ENST00000584450.5:c.3160-187G= ENSP00000463714.1:n.3160-187G=
ENST00000584601.5:c.3277G= ENSP00000462438.1:p.Glu1093=
NM_001005862.2:c.3277G= , LRG_724t1:c.3277G= NP_001005862.1:p.Glu1093=
NM_001289936.1:c.3322G= , LRG_724t4:c.3322G= NP_001276865.1:p.Glu1108=
NM_001289937.1:c.3160-187G= NP_001276866.1:n.3160-187G=
NM_004448.3:c.3367G= , LRG_724t2:c.3367G= NP_004439.2:p.Glu1123=
NR_110535.1:n.3691G=
XM_024450641.1:c.3505G= XP_024306409.1:p.Glu1169=
XM_024450642.1:c.3460G= XP_024306410.1:p.Glu1154=
XM_024450643.1:c.3415G= XP_024306411.1:p.Glu1139=
NM_001005862.3:c.3277G= NP_001005862.1:p.Glu1093=
NM_001289936.2:c.3322G= NP_001276865.1:p.Glu1108=
NM_001289937.2:c.3160-187G= NP_001276866.1:n.3160-187G=
NM_001382782.1:c.3277G= NP_001369711.1:p.Glu1093=
NM_001382783.1:c.3277G= NP_001369712.1:p.Glu1093=
NM_001382784.1:c.3484G= NP_001369713.1:p.Glu1162=
NM_001382785.1:c.3469G= NP_001369714.1:p.Glu1157=
NM_001382786.1:c.3448G= NP_001369715.1:p.Glu1150=
NM_001382787.1:c.3442G= NP_001369716.1:p.Glu1148=
NM_001382788.1:c.3397G= NP_001369717.1:p.Glu1133=
NM_001382789.1:c.3388G= NP_001369718.1:p.Glu1130=
NM_001382790.1:c.3364G= NP_001369719.1:p.Glu1122=
NM_001382791.1:c.3358G= NP_001369720.1:p.Glu1120=
NM_001382792.1:c.3331G= NP_001369721.1:p.Glu1111=
NM_001382793.1:c.3325G= NP_001369722.1:p.Glu1109=
NM_001382794.1:c.3325G= NP_001369723.1:p.Glu1109=
NM_001382795.1:c.3319G= NP_001369724.1:p.Glu1107=
NM_001382796.1:c.3280G= NP_001369725.1:p.Glu1094=
NM_001382797.1:c.3268G= NP_001369726.1:p.Glu1090=
NM_001382798.1:c.3211G= NP_001369727.1:p.Glu1071=
NM_001382799.1:c.3187G= NP_001369728.1:p.Glu1063=
NM_001382800.1:c.3181G= NP_001369729.1:p.Glu1061=
NM_001382801.1:c.3163G= NP_001369730.1:p.Glu1055=
NM_001382802.1:c.3109G= NP_001369731.1:p.Glu1037=
NM_001382803.1:c.3118-187G= NP_001369732.1:n.3118-187G=
NM_001382804.1:c.2539G= NP_001369733.1:p.Glu847=
NM_001382805.1:c.2416G= NP_001369734.1:p.Glu806=
NM_001382806.1:c.2329G= NP_001369735.1:p.Glu777=
NM_004448.4:c.3367G= MANE Select NP_004439.2:p.Glu1123=
NR_110535.2:n.3605G=