Canonical Allele Identifier: CA399303047
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724782C>G , CM000679.2:g.39724782C>G GRCh38
NC_000017.10:g.37881035C>G , CM000679.1:g.37881035C>G GRCh37
NC_000017.9:g.35134561C>G NCBI36
NG_007503.1:g.41643C>G , LRG_724:g.41643C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2364C>G MANE Select ENSP00000269571.4:p.Ile788Met
ENST00000269571.9:c.2364C>G ENSP00000269571.4:p.Ile788Met
ENST00000406381.6:c.2274C>G ENSP00000385185.2:p.Ile758Met
ENST00000445658.6:c.1536C>G ENSP00000404047.2:p.Ile512Met
ENST00000541774.5:c.2319C>G ENSP00000446466.1:p.Ile773Met
ENST00000578373.5:c.*2154C>G ENSP00000463427.1:n.*2154C>G
ENST00000580074.1:c.470C>G
ENST00000583038.5:n.3498C>G
ENST00000584450.5:c.2364C>G ENSP00000463714.1:p.Ile788Met
ENST00000584601.5:c.2274C>G ENSP00000462438.1:p.Ile758Met
NM_001005862.2:c.2274C>G , LRG_724t1:c.2274C>G NP_001005862.1:p.Ile758Met
NM_001289936.1:c.2319C>G , LRG_724t4:c.2319C>G NP_001276865.1:p.Ile773Met
NM_001289937.1:c.2364C>G NP_001276866.1:p.Ile788Met
NM_004448.3:c.2364C>G , LRG_724t2:c.2364C>G NP_004439.2:p.Ile788Met
NR_110535.1:n.2688C>G
XM_024450641.1:c.2502C>G XP_024306409.1:p.Ile834Met
XM_024450642.1:c.2457C>G XP_024306410.1:p.Ile819Met
XM_024450643.1:c.2412C>G XP_024306411.1:p.Ile804Met
NM_001005862.3:c.2274C>G NP_001005862.1:p.Ile758Met
NM_001289936.2:c.2319C>G NP_001276865.1:p.Ile773Met
NM_001289937.2:c.2364C>G NP_001276866.1:p.Ile788Met
NM_001382782.1:c.2274C>G NP_001369711.1:p.Ile758Met
NM_001382783.1:c.2274C>G NP_001369712.1:p.Ile758Met
NM_001382784.1:c.2481C>G NP_001369713.1:p.Ile827Met
NM_001382785.1:c.2466C>G NP_001369714.1:p.Ile822Met
NM_001382786.1:c.2445C>G NP_001369715.1:p.Ile815Met
NM_001382787.1:c.2439C>G NP_001369716.1:p.Ile813Met
NM_001382788.1:c.2394C>G NP_001369717.1:p.Ile798Met
NM_001382789.1:c.2385C>G NP_001369718.1:p.Ile795Met
NM_001382790.1:c.2361C>G NP_001369719.1:p.Ile787Met
NM_001382791.1:c.2355C>G NP_001369720.1:p.Ile785Met
NM_001382792.1:c.2328C>G NP_001369721.1:p.Ile776Met
NM_001382793.1:c.2322C>G NP_001369722.1:p.Ile774Met
NM_001382794.1:c.2322C>G NP_001369723.1:p.Ile774Met
NM_001382795.1:c.2316C>G NP_001369724.1:p.Ile772Met
NM_001382796.1:c.2364C>G NP_001369725.1:p.Ile788Met
NM_001382797.1:c.2265C>G NP_001369726.1:p.Ile755Met
NM_001382798.1:c.2364C>G NP_001369727.1:p.Ile788Met
NM_001382799.1:c.2184C>G NP_001369728.1:p.Ile728Met
NM_001382800.1:c.2308-267C>G NP_001369729.1:n.2308-267C>G
NM_001382801.1:c.2316C>G NP_001369730.1:p.Ile772Met
NM_001382802.1:c.2106C>G NP_001369731.1:p.Ile702Met
NM_001382803.1:c.2322C>G NP_001369732.1:p.Ile774Met
NM_001382804.1:c.1536C>G NP_001369733.1:p.Ile512Met
NM_001382805.1:c.2208+1122C>G NP_001369734.1:n.2208+1122C>G
NM_001382806.1:c.1326C>G NP_001369735.1:p.Ile442Met
NM_004448.4:c.2364C>G MANE Select NP_004439.2:p.Ile788Met
NR_110535.2:n.2602C>G