Canonical Allele Identifier: CA2259229269
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727803G= , CM000679.2:g.39727803G= GRCh38
NC_000017.10:g.37884056G= , CM000679.1:g.37884056G= GRCh37
NC_000017.9:g.35137582G= NCBI36
NG_007503.1:g.44664G= , LRG_724:g.44664G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3527G= MANE Select ENSP00000269571.4:p.Gly1176=
ENST00000269571.9:c.3527G= ENSP00000269571.4:p.Gly1176=
ENST00000406381.6:c.3437G= ENSP00000385185.2:p.Gly1146=
ENST00000445658.6:c.2699G= ENSP00000404047.2:p.Gly900=
ENST00000541774.5:c.3482G= ENSP00000446466.1:p.Gly1161=
ENST00000578373.5:c.*3317G= ENSP00000463427.1:n.*3317G=
ENST00000584450.5:c.*106G= ENSP00000463714.1:n.*106G=
ENST00000584601.5:c.3437G= ENSP00000462438.1:p.Gly1146=
NM_001005862.2:c.3437G= , LRG_724t1:c.3437G= NP_001005862.1:p.Gly1146=
NM_001289936.1:c.3482G= , LRG_724t4:c.3482G= NP_001276865.1:p.Gly1161=
NM_001289937.1:c.*106G= NP_001276866.1:n.*106G=
NM_004448.3:c.3527G= , LRG_724t2:c.3527G= NP_004439.2:p.Gly1176=
NR_110535.1:n.3851G=
XM_024450641.1:c.3665G= XP_024306409.1:p.Gly1222=
XM_024450642.1:c.3620G= XP_024306410.1:p.Gly1207=
XM_024450643.1:c.3575G= XP_024306411.1:p.Gly1192=
NM_001005862.3:c.3437G= NP_001005862.1:p.Gly1146=
NM_001289936.2:c.3482G= NP_001276865.1:p.Gly1161=
NM_001289937.2:c.*106G= NP_001276866.1:n.*106G=
NM_001382782.1:c.3437G= NP_001369711.1:p.Gly1146=
NM_001382783.1:c.3437G= NP_001369712.1:p.Gly1146=
NM_001382784.1:c.3644G= NP_001369713.1:p.Gly1215=
NM_001382785.1:c.3629G= NP_001369714.1:p.Gly1210=
NM_001382786.1:c.3608G= NP_001369715.1:p.Gly1203=
NM_001382787.1:c.3602G= NP_001369716.1:p.Gly1201=
NM_001382788.1:c.3557G= NP_001369717.1:p.Gly1186=
NM_001382789.1:c.3548G= NP_001369718.1:p.Gly1183=
NM_001382790.1:c.3524G= NP_001369719.1:p.Gly1175=
NM_001382791.1:c.3518G= NP_001369720.1:p.Gly1173=
NM_001382792.1:c.3491G= NP_001369721.1:p.Gly1164=
NM_001382793.1:c.3485G= NP_001369722.1:p.Gly1162=
NM_001382794.1:c.3485G= NP_001369723.1:p.Gly1162=
NM_001382795.1:c.3479G= NP_001369724.1:p.Gly1160=
NM_001382796.1:c.3440G= NP_001369725.1:p.Gly1147=
NM_001382797.1:c.3428G= NP_001369726.1:p.Gly1143=
NM_001382798.1:c.3371G= NP_001369727.1:p.Gly1124=
NM_001382799.1:c.3347G= NP_001369728.1:p.Gly1116=
NM_001382800.1:c.3341G= NP_001369729.1:p.Gly1114=
NM_001382801.1:c.3323G= NP_001369730.1:p.Gly1108=
NM_001382802.1:c.3269G= NP_001369731.1:p.Gly1090=
NM_001382803.1:c.*106G= NP_001369732.1:n.*106G=
NM_001382804.1:c.2699G= NP_001369733.1:p.Gly900=
NM_001382805.1:c.2576G= NP_001369734.1:p.Gly859=
NM_001382806.1:c.2489G= NP_001369735.1:p.Gly830=
NM_004448.4:c.3527G= MANE Select NP_004439.2:p.Gly1176=
NR_110535.2:n.3765G=