Canonical Allele Identifier: CA399303090
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145849536

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724789A>G , CM000679.2:g.39724789A>G GRCh38
NC_000017.10:g.37881042A>G , CM000679.1:g.37881042A>G GRCh37
NC_000017.9:g.35134568A>G NCBI36
NG_007503.1:g.41650A>G , LRG_724:g.41650A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2371A>G MANE Select ENSP00000269571.4:p.Thr791Ala
ENST00000269571.9:c.2371A>G ENSP00000269571.4:p.Thr791Ala
ENST00000406381.6:c.2281A>G ENSP00000385185.2:p.Thr761Ala
ENST00000445658.6:c.1543A>G ENSP00000404047.2:p.Thr515Ala
ENST00000541774.5:c.2326A>G ENSP00000446466.1:p.Thr776Ala
ENST00000578373.5:c.*2161A>G ENSP00000463427.1:n.*2161A>G
ENST00000580074.1:c.477A>G
ENST00000583038.5:n.3505A>G
ENST00000584450.5:c.2371A>G ENSP00000463714.1:p.Thr791Ala
ENST00000584601.5:c.2281A>G ENSP00000462438.1:p.Thr761Ala
NM_001005862.2:c.2281A>G , LRG_724t1:c.2281A>G NP_001005862.1:p.Thr761Ala
NM_001289936.1:c.2326A>G , LRG_724t4:c.2326A>G NP_001276865.1:p.Thr776Ala
NM_001289937.1:c.2371A>G NP_001276866.1:p.Thr791Ala
NM_004448.3:c.2371A>G , LRG_724t2:c.2371A>G NP_004439.2:p.Thr791Ala
NR_110535.1:n.2695A>G
XM_024450641.1:c.2509A>G XP_024306409.1:p.Thr837Ala
XM_024450642.1:c.2464A>G XP_024306410.1:p.Thr822Ala
XM_024450643.1:c.2419A>G XP_024306411.1:p.Thr807Ala
NM_001005862.3:c.2281A>G NP_001005862.1:p.Thr761Ala
NM_001289936.2:c.2326A>G NP_001276865.1:p.Thr776Ala
NM_001289937.2:c.2371A>G NP_001276866.1:p.Thr791Ala
NM_001382782.1:c.2281A>G NP_001369711.1:p.Thr761Ala
NM_001382783.1:c.2281A>G NP_001369712.1:p.Thr761Ala
NM_001382784.1:c.2488A>G NP_001369713.1:p.Thr830Ala
NM_001382785.1:c.2473A>G NP_001369714.1:p.Thr825Ala
NM_001382786.1:c.2452A>G NP_001369715.1:p.Thr818Ala
NM_001382787.1:c.2446A>G NP_001369716.1:p.Thr816Ala
NM_001382788.1:c.2401A>G NP_001369717.1:p.Thr801Ala
NM_001382789.1:c.2392A>G NP_001369718.1:p.Thr798Ala
NM_001382790.1:c.2368A>G NP_001369719.1:p.Thr790Ala
NM_001382791.1:c.2362A>G NP_001369720.1:p.Thr788Ala
NM_001382792.1:c.2335A>G NP_001369721.1:p.Thr779Ala
NM_001382793.1:c.2329A>G NP_001369722.1:p.Thr777Ala
NM_001382794.1:c.2329A>G NP_001369723.1:p.Thr777Ala
NM_001382795.1:c.2323A>G NP_001369724.1:p.Thr775Ala
NM_001382796.1:c.2371A>G NP_001369725.1:p.Thr791Ala
NM_001382797.1:c.2272A>G NP_001369726.1:p.Thr758Ala
NM_001382798.1:c.2371A>G NP_001369727.1:p.Thr791Ala
NM_001382799.1:c.2191A>G NP_001369728.1:p.Thr731Ala
NM_001382800.1:c.2308-260A>G NP_001369729.1:n.2308-260A>G
NM_001382801.1:c.2323A>G NP_001369730.1:p.Thr775Ala
NM_001382802.1:c.2113A>G NP_001369731.1:p.Thr705Ala
NM_001382803.1:c.2329A>G NP_001369732.1:p.Thr777Ala
NM_001382804.1:c.1543A>G NP_001369733.1:p.Thr515Ala
NM_001382805.1:c.2208+1129A>G NP_001369734.1:n.2208+1129A>G
NM_001382806.1:c.1333A>G NP_001369735.1:p.Thr445Ala
NM_004448.4:c.2371A>G MANE Select NP_004439.2:p.Thr791Ala
NR_110535.2:n.2609A>G