Canonical Allele Identifier: CA399303026
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145849122

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724778G>C , CM000679.2:g.39724778G>C GRCh38
NC_000017.10:g.37881031G>C , CM000679.1:g.37881031G>C GRCh37
NC_000017.9:g.35134557G>C NCBI36
NG_007503.1:g.41639G>C , LRG_724:g.41639G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2360G>C MANE Select ENSP00000269571.4:p.Gly787Ala
ENST00000269571.9:c.2360G>C ENSP00000269571.4:p.Gly787Ala
ENST00000406381.6:c.2270G>C ENSP00000385185.2:p.Gly757Ala
ENST00000445658.6:c.1532G>C ENSP00000404047.2:p.Gly511Ala
ENST00000541774.5:c.2315G>C ENSP00000446466.1:p.Gly772Ala
ENST00000578373.5:c.*2150G>C ENSP00000463427.1:n.*2150G>C
ENST00000580074.1:c.466G>C
ENST00000583038.5:n.3494G>C
ENST00000584450.5:c.2360G>C ENSP00000463714.1:p.Gly787Ala
ENST00000584601.5:c.2270G>C ENSP00000462438.1:p.Gly757Ala
NM_001005862.2:c.2270G>C , LRG_724t1:c.2270G>C NP_001005862.1:p.Gly757Ala
NM_001289936.1:c.2315G>C , LRG_724t4:c.2315G>C NP_001276865.1:p.Gly772Ala
NM_001289937.1:c.2360G>C NP_001276866.1:p.Gly787Ala
NM_004448.3:c.2360G>C , LRG_724t2:c.2360G>C NP_004439.2:p.Gly787Ala
NR_110535.1:n.2684G>C
XM_024450641.1:c.2498G>C XP_024306409.1:p.Gly833Ala
XM_024450642.1:c.2453G>C XP_024306410.1:p.Gly818Ala
XM_024450643.1:c.2408G>C XP_024306411.1:p.Gly803Ala
NM_001005862.3:c.2270G>C NP_001005862.1:p.Gly757Ala
NM_001289936.2:c.2315G>C NP_001276865.1:p.Gly772Ala
NM_001289937.2:c.2360G>C NP_001276866.1:p.Gly787Ala
NM_001382782.1:c.2270G>C NP_001369711.1:p.Gly757Ala
NM_001382783.1:c.2270G>C NP_001369712.1:p.Gly757Ala
NM_001382784.1:c.2477G>C NP_001369713.1:p.Gly826Ala
NM_001382785.1:c.2462G>C NP_001369714.1:p.Gly821Ala
NM_001382786.1:c.2441G>C NP_001369715.1:p.Gly814Ala
NM_001382787.1:c.2435G>C NP_001369716.1:p.Gly812Ala
NM_001382788.1:c.2390G>C NP_001369717.1:p.Gly797Ala
NM_001382789.1:c.2381G>C NP_001369718.1:p.Gly794Ala
NM_001382790.1:c.2357G>C NP_001369719.1:p.Gly786Ala
NM_001382791.1:c.2351G>C NP_001369720.1:p.Gly784Ala
NM_001382792.1:c.2324G>C NP_001369721.1:p.Gly775Ala
NM_001382793.1:c.2318G>C NP_001369722.1:p.Gly773Ala
NM_001382794.1:c.2318G>C NP_001369723.1:p.Gly773Ala
NM_001382795.1:c.2312G>C NP_001369724.1:p.Gly771Ala
NM_001382796.1:c.2360G>C NP_001369725.1:p.Gly787Ala
NM_001382797.1:c.2261G>C NP_001369726.1:p.Gly754Ala
NM_001382798.1:c.2360G>C NP_001369727.1:p.Gly787Ala
NM_001382799.1:c.2180G>C NP_001369728.1:p.Gly727Ala
NM_001382800.1:c.2308-271G>C NP_001369729.1:n.2308-271G>C
NM_001382801.1:c.2312G>C NP_001369730.1:p.Gly771Ala
NM_001382802.1:c.2102G>C NP_001369731.1:p.Gly701Ala
NM_001382803.1:c.2318G>C NP_001369732.1:p.Gly773Ala
NM_001382804.1:c.1532G>C NP_001369733.1:p.Gly511Ala
NM_001382805.1:c.2208+1118G>C NP_001369734.1:n.2208+1118G>C
NM_001382806.1:c.1322G>C NP_001369735.1:p.Gly441Ala
NM_004448.4:c.2360G>C MANE Select NP_004439.2:p.Gly787Ala
NR_110535.2:n.2598G>C