Canonical Allele Identifier: CA2259222382
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39712051C= , CM000679.2:g.39712051C= GRCh38
NC_000017.10:g.37868304C= , CM000679.1:g.37868304C= GRCh37
NC_000017.9:g.35121830C= NCBI36
NG_007503.1:g.28912C= , LRG_724:g.28912C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.1021+4C= MANE Select ENSP00000269571.4:n.1021+4C=
ENST00000269571.9:c.1021+4C= ENSP00000269571.4:n.1021+4C=
ENST00000406381.6:c.931+4C= ENSP00000385185.2:n.931+4C=
ENST00000445658.6:c.193+4C= ENSP00000404047.2:n.193+4C=
ENST00000541774.5:c.976+4C= ENSP00000446466.1:n.976+4C=
ENST00000578199.5:c.931+4C= ENSP00000462808.1:n.931+4C=
ENST00000578373.5:c.*811+4C= ENSP00000463427.1:n.*811+4C=
ENST00000578502.1:c.246+4C=
ENST00000582648.5:c.*54+4C= ENSP00000462024.1:n.*54+4C=
ENST00000582788.5:n.510+4C=
ENST00000583038.5:n.1713+4C=
ENST00000584450.5:c.1021+4C= ENSP00000463714.1:n.1021+4C=
ENST00000584601.5:c.931+4C= ENSP00000462438.1:n.931+4C=
ENST00000584908.5:n.1037C=
NM_001005862.2:c.931+4C= , LRG_724t1:c.931+4C= NP_001005862.1:n.931+4C=
NM_001289936.1:c.976+4C= , LRG_724t4:c.976+4C= NP_001276865.1:n.976+4C=
NM_001289937.1:c.1021+4C= NP_001276866.1:n.1021+4C=
NM_001289938.1:c.931+4C= , LRG_724t3:c.931+4C= NP_001276867.1:n.931+4C=
NM_004448.3:c.1021+4C= , LRG_724t2:c.1021+4C= NP_004439.2:n.1021+4C=
NR_110535.1:n.1345+4C=
XM_024450641.1:c.1159+4C= XP_024306409.1:n.1159+4C=
XM_024450642.1:c.1114+4C= XP_024306410.1:n.1114+4C=
XM_024450643.1:c.1069+4C= XP_024306411.1:n.1069+4C=
NM_001005862.3:c.931+4C= NP_001005862.1:n.931+4C=
NM_001289936.2:c.976+4C= NP_001276865.1:n.976+4C=
NM_001289937.2:c.1021+4C= NP_001276866.1:n.1021+4C=
NM_001289938.2:c.931+4C= NP_001276867.1:n.931+4C=
NM_001382782.1:c.931+4C= NP_001369711.1:n.931+4C=
NM_001382783.1:c.931+4C= NP_001369712.1:n.931+4C=
NM_001382784.1:c.1021+4C= NP_001369713.1:n.1021+4C=
NM_001382785.1:c.1021+4C= NP_001369714.1:n.1021+4C=
NM_001382786.1:c.1021+4C= NP_001369715.1:n.1021+4C=
NM_001382787.1:c.1096+4C= NP_001369716.1:n.1096+4C=
NM_001382788.1:c.1021+4C= NP_001369717.1:n.1021+4C=
NM_001382789.1:c.1021+4C= NP_001369718.1:n.1021+4C=
NM_001382790.1:c.1021+4C= NP_001369719.1:n.1021+4C=
NM_001382791.1:c.1012+4C= NP_001369720.1:n.1012+4C=
NM_001382792.1:c.1021+4C= NP_001369721.1:n.1021+4C=
NM_001382793.1:c.1021+4C= NP_001369722.1:n.1021+4C=
NM_001382794.1:c.1021+4C= NP_001369723.1:n.1021+4C=
NM_001382795.1:c.1021+4C= NP_001369724.1:n.1021+4C=
NM_001382796.1:c.1021+4C= NP_001369725.1:n.1021+4C=
NM_001382797.1:c.1021+4C= NP_001369726.1:n.1021+4C=
NM_001382798.1:c.1021+4C= NP_001369727.1:n.1021+4C=
NM_001382799.1:c.841+4C= NP_001369728.1:n.841+4C=
NM_001382800.1:c.1021+4C= NP_001369729.1:n.1021+4C=
NM_001382801.1:c.1021+4C= NP_001369730.1:n.1021+4C=
NM_001382802.1:c.763+4C= NP_001369731.1:n.763+4C=
NM_001382803.1:c.1021+4C= NP_001369732.1:n.1021+4C=
NM_001382804.1:c.193+4C= NP_001369733.1:n.193+4C=
NM_001382805.1:c.1021+4C= NP_001369734.1:n.1021+4C=
NM_001382806.1:c.1021+4C= NP_001369735.1:n.1021+4C=
NM_004448.4:c.1021+4C= MANE Select NP_004439.2:n.1021+4C=
NR_110535.2:n.1259+4C=