Canonical Allele Identifier: CA2259228834
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727481C= , CM000679.2:g.39727481C= GRCh38
NC_000017.10:g.37883734C= , CM000679.1:g.37883734C= GRCh37
NC_000017.9:g.35137260C= NCBI36
NG_007503.1:g.44342C= , LRG_724:g.44342C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3346C= MANE Select ENSP00000269571.4:p.Pro1116=
ENST00000269571.9:c.3346C= ENSP00000269571.4:p.Pro1116=
ENST00000406381.6:c.3256C= ENSP00000385185.2:p.Pro1086=
ENST00000445658.6:c.2518C= ENSP00000404047.2:p.Pro840=
ENST00000541774.5:c.3301C= ENSP00000446466.1:p.Pro1101=
ENST00000578373.5:c.*3136C= ENSP00000463427.1:n.*3136C=
ENST00000584450.5:c.3160-208C= ENSP00000463714.1:n.3160-208C=
ENST00000584601.5:c.3256C= ENSP00000462438.1:p.Pro1086=
NM_001005862.2:c.3256C= , LRG_724t1:c.3256C= NP_001005862.1:p.Pro1086=
NM_001289936.1:c.3301C= , LRG_724t4:c.3301C= NP_001276865.1:p.Pro1101=
NM_001289937.1:c.3160-208C= NP_001276866.1:n.3160-208C=
NM_004448.3:c.3346C= , LRG_724t2:c.3346C= NP_004439.2:p.Pro1116=
NR_110535.1:n.3670C=
XM_024450641.1:c.3484C= XP_024306409.1:p.Pro1162=
XM_024450642.1:c.3439C= XP_024306410.1:p.Pro1147=
XM_024450643.1:c.3394C= XP_024306411.1:p.Pro1132=
NM_001005862.3:c.3256C= NP_001005862.1:p.Pro1086=
NM_001289936.2:c.3301C= NP_001276865.1:p.Pro1101=
NM_001289937.2:c.3160-208C= NP_001276866.1:n.3160-208C=
NM_001382782.1:c.3256C= NP_001369711.1:p.Pro1086=
NM_001382783.1:c.3256C= NP_001369712.1:p.Pro1086=
NM_001382784.1:c.3463C= NP_001369713.1:p.Pro1155=
NM_001382785.1:c.3448C= NP_001369714.1:p.Pro1150=
NM_001382786.1:c.3427C= NP_001369715.1:p.Pro1143=
NM_001382787.1:c.3421C= NP_001369716.1:p.Pro1141=
NM_001382788.1:c.3376C= NP_001369717.1:p.Pro1126=
NM_001382789.1:c.3367C= NP_001369718.1:p.Pro1123=
NM_001382790.1:c.3343C= NP_001369719.1:p.Pro1115=
NM_001382791.1:c.3337C= NP_001369720.1:p.Pro1113=
NM_001382792.1:c.3310C= NP_001369721.1:p.Pro1104=
NM_001382793.1:c.3304C= NP_001369722.1:p.Pro1102=
NM_001382794.1:c.3304C= NP_001369723.1:p.Pro1102=
NM_001382795.1:c.3298C= NP_001369724.1:p.Pro1100=
NM_001382796.1:c.3259C= NP_001369725.1:p.Pro1087=
NM_001382797.1:c.3247C= NP_001369726.1:p.Pro1083=
NM_001382798.1:c.3190C= NP_001369727.1:p.Pro1064=
NM_001382799.1:c.3166C= NP_001369728.1:p.Pro1056=
NM_001382800.1:c.3160C= NP_001369729.1:p.Pro1054=
NM_001382801.1:c.3142C= NP_001369730.1:p.Pro1048=
NM_001382802.1:c.3088C= NP_001369731.1:p.Pro1030=
NM_001382803.1:c.3118-208C= NP_001369732.1:n.3118-208C=
NM_001382804.1:c.2518C= NP_001369733.1:p.Pro840=
NM_001382805.1:c.2395C= NP_001369734.1:p.Pro799=
NM_001382806.1:c.2308C= NP_001369735.1:p.Pro770=
NM_004448.4:c.3346C= MANE Select NP_004439.2:p.Pro1116=
NR_110535.2:n.3584C=