Canonical Allele Identifier: CA2259229230
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727721C= , CM000679.2:g.39727721C= GRCh38
NC_000017.10:g.37883974C= , CM000679.1:g.37883974C= GRCh37
NC_000017.9:g.35137500C= NCBI36
NG_007503.1:g.44582C= , LRG_724:g.44582C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3445C= MANE Select ENSP00000269571.4:p.Pro1149=
ENST00000269571.9:c.3445C= ENSP00000269571.4:p.Pro1149=
ENST00000406381.6:c.3355C= ENSP00000385185.2:p.Pro1119=
ENST00000445658.6:c.2617C= ENSP00000404047.2:p.Pro873=
ENST00000541774.5:c.3400C= ENSP00000446466.1:p.Pro1134=
ENST00000578373.5:c.*3235C= ENSP00000463427.1:n.*3235C=
ENST00000584450.5:c.*24C= ENSP00000463714.1:n.*24C=
ENST00000584601.5:c.3355C= ENSP00000462438.1:p.Pro1119=
NM_001005862.2:c.3355C= , LRG_724t1:c.3355C= NP_001005862.1:p.Pro1119=
NM_001289936.1:c.3400C= , LRG_724t4:c.3400C= NP_001276865.1:p.Pro1134=
NM_001289937.1:c.*24C= NP_001276866.1:n.*24C=
NM_004448.3:c.3445C= , LRG_724t2:c.3445C= NP_004439.2:p.Pro1149=
NR_110535.1:n.3769C=
XM_024450641.1:c.3583C= XP_024306409.1:p.Pro1195=
XM_024450642.1:c.3538C= XP_024306410.1:p.Pro1180=
XM_024450643.1:c.3493C= XP_024306411.1:p.Pro1165=
NM_001005862.3:c.3355C= NP_001005862.1:p.Pro1119=
NM_001289936.2:c.3400C= NP_001276865.1:p.Pro1134=
NM_001289937.2:c.*24C= NP_001276866.1:n.*24C=
NM_001382782.1:c.3355C= NP_001369711.1:p.Pro1119=
NM_001382783.1:c.3355C= NP_001369712.1:p.Pro1119=
NM_001382784.1:c.3562C= NP_001369713.1:p.Pro1188=
NM_001382785.1:c.3547C= NP_001369714.1:p.Pro1183=
NM_001382786.1:c.3526C= NP_001369715.1:p.Pro1176=
NM_001382787.1:c.3520C= NP_001369716.1:p.Pro1174=
NM_001382788.1:c.3475C= NP_001369717.1:p.Pro1159=
NM_001382789.1:c.3466C= NP_001369718.1:p.Pro1156=
NM_001382790.1:c.3442C= NP_001369719.1:p.Pro1148=
NM_001382791.1:c.3436C= NP_001369720.1:p.Pro1146=
NM_001382792.1:c.3409C= NP_001369721.1:p.Pro1137=
NM_001382793.1:c.3403C= NP_001369722.1:p.Pro1135=
NM_001382794.1:c.3403C= NP_001369723.1:p.Pro1135=
NM_001382795.1:c.3397C= NP_001369724.1:p.Pro1133=
NM_001382796.1:c.3358C= NP_001369725.1:p.Pro1120=
NM_001382797.1:c.3346C= NP_001369726.1:p.Pro1116=
NM_001382798.1:c.3289C= NP_001369727.1:p.Pro1097=
NM_001382799.1:c.3265C= NP_001369728.1:p.Pro1089=
NM_001382800.1:c.3259C= NP_001369729.1:p.Pro1087=
NM_001382801.1:c.3241C= NP_001369730.1:p.Pro1081=
NM_001382802.1:c.3187C= NP_001369731.1:p.Pro1063=
NM_001382803.1:c.*24C= NP_001369732.1:n.*24C=
NM_001382804.1:c.2617C= NP_001369733.1:p.Pro873=
NM_001382805.1:c.2494C= NP_001369734.1:p.Pro832=
NM_001382806.1:c.2407C= NP_001369735.1:p.Pro803=
NM_004448.4:c.3445C= MANE Select NP_004439.2:p.Pro1149=
NR_110535.2:n.3683C=