Canonical Allele Identifier: CA2259229141
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727517G= , CM000679.2:g.39727517G= GRCh38
NC_000017.10:g.37883770G= , CM000679.1:g.37883770G= GRCh37
NC_000017.9:g.35137296G= NCBI36
NG_007503.1:g.44378G= , LRG_724:g.44378G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3382G= MANE Select ENSP00000269571.4:p.Val1128=
ENST00000269571.9:c.3382G= ENSP00000269571.4:p.Val1128=
ENST00000406381.6:c.3292G= ENSP00000385185.2:p.Val1098=
ENST00000445658.6:c.2554G= ENSP00000404047.2:p.Val852=
ENST00000541774.5:c.3337G= ENSP00000446466.1:p.Val1113=
ENST00000578373.5:c.*3172G= ENSP00000463427.1:n.*3172G=
ENST00000584450.5:c.3160-172G= ENSP00000463714.1:n.3160-172G=
ENST00000584601.5:c.3292G= ENSP00000462438.1:p.Val1098=
NM_001005862.2:c.3292G= , LRG_724t1:c.3292G= NP_001005862.1:p.Val1098=
NM_001289936.1:c.3337G= , LRG_724t4:c.3337G= NP_001276865.1:p.Val1113=
NM_001289937.1:c.3160-172G= NP_001276866.1:n.3160-172G=
NM_004448.3:c.3382G= , LRG_724t2:c.3382G= NP_004439.2:p.Val1128=
NR_110535.1:n.3706G=
XM_024450641.1:c.3520G= XP_024306409.1:p.Val1174=
XM_024450642.1:c.3475G= XP_024306410.1:p.Val1159=
XM_024450643.1:c.3430G= XP_024306411.1:p.Val1144=
NM_001005862.3:c.3292G= NP_001005862.1:p.Val1098=
NM_001289936.2:c.3337G= NP_001276865.1:p.Val1113=
NM_001289937.2:c.3160-172G= NP_001276866.1:n.3160-172G=
NM_001382782.1:c.3292G= NP_001369711.1:p.Val1098=
NM_001382783.1:c.3292G= NP_001369712.1:p.Val1098=
NM_001382784.1:c.3499G= NP_001369713.1:p.Val1167=
NM_001382785.1:c.3484G= NP_001369714.1:p.Val1162=
NM_001382786.1:c.3463G= NP_001369715.1:p.Val1155=
NM_001382787.1:c.3457G= NP_001369716.1:p.Val1153=
NM_001382788.1:c.3412G= NP_001369717.1:p.Val1138=
NM_001382789.1:c.3403G= NP_001369718.1:p.Val1135=
NM_001382790.1:c.3379G= NP_001369719.1:p.Val1127=
NM_001382791.1:c.3373G= NP_001369720.1:p.Val1125=
NM_001382792.1:c.3346G= NP_001369721.1:p.Val1116=
NM_001382793.1:c.3340G= NP_001369722.1:p.Val1114=
NM_001382794.1:c.3340G= NP_001369723.1:p.Val1114=
NM_001382795.1:c.3334G= NP_001369724.1:p.Val1112=
NM_001382796.1:c.3295G= NP_001369725.1:p.Val1099=
NM_001382797.1:c.3283G= NP_001369726.1:p.Val1095=
NM_001382798.1:c.3226G= NP_001369727.1:p.Val1076=
NM_001382799.1:c.3202G= NP_001369728.1:p.Val1068=
NM_001382800.1:c.3196G= NP_001369729.1:p.Val1066=
NM_001382801.1:c.3178G= NP_001369730.1:p.Val1060=
NM_001382802.1:c.3124G= NP_001369731.1:p.Val1042=
NM_001382803.1:c.3118-172G= NP_001369732.1:n.3118-172G=
NM_001382804.1:c.2554G= NP_001369733.1:p.Val852=
NM_001382805.1:c.2431G= NP_001369734.1:p.Val811=
NM_001382806.1:c.2344G= NP_001369735.1:p.Val782=
NM_004448.4:c.3382G= MANE Select NP_004439.2:p.Val1128=
NR_110535.2:n.3620G=