Canonical Allele Identifier: CA399302798
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145846948

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724733A>T , CM000679.2:g.39724733A>T GRCh38
NC_000017.10:g.37880986A>T , CM000679.1:g.37880986A>T GRCh37
NC_000017.9:g.35134512A>T NCBI36
NG_007503.1:g.41594A>T , LRG_724:g.41594A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2315A>T MANE Select ENSP00000269571.4:p.Tyr772Phe
ENST00000269571.9:c.2315A>T ENSP00000269571.4:p.Tyr772Phe
ENST00000406381.6:c.2225A>T ENSP00000385185.2:p.Tyr742Phe
ENST00000445658.6:c.1487A>T ENSP00000404047.2:p.Tyr496Phe
ENST00000541774.5:c.2270A>T ENSP00000446466.1:p.Tyr757Phe
ENST00000578373.5:c.*2105A>T ENSP00000463427.1:n.*2105A>T
ENST00000580074.1:c.421A>T
ENST00000583038.5:n.3449A>T
ENST00000584450.5:c.2315A>T ENSP00000463714.1:p.Tyr772Phe
ENST00000584601.5:c.2225A>T ENSP00000462438.1:p.Tyr742Phe
NM_001005862.2:c.2225A>T , LRG_724t1:c.2225A>T NP_001005862.1:p.Tyr742Phe
NM_001289936.1:c.2270A>T , LRG_724t4:c.2270A>T NP_001276865.1:p.Tyr757Phe
NM_001289937.1:c.2315A>T NP_001276866.1:p.Tyr772Phe
NM_004448.3:c.2315A>T , LRG_724t2:c.2315A>T NP_004439.2:p.Tyr772Phe
NR_110535.1:n.2639A>T
XM_024450641.1:c.2453A>T XP_024306409.1:p.Tyr818Phe
XM_024450642.1:c.2408A>T XP_024306410.1:p.Tyr803Phe
XM_024450643.1:c.2363A>T XP_024306411.1:p.Tyr788Phe
NM_001005862.3:c.2225A>T NP_001005862.1:p.Tyr742Phe
NM_001289936.2:c.2270A>T NP_001276865.1:p.Tyr757Phe
NM_001289937.2:c.2315A>T NP_001276866.1:p.Tyr772Phe
NM_001382782.1:c.2225A>T NP_001369711.1:p.Tyr742Phe
NM_001382783.1:c.2225A>T NP_001369712.1:p.Tyr742Phe
NM_001382784.1:c.2432A>T NP_001369713.1:p.Tyr811Phe
NM_001382785.1:c.2417A>T NP_001369714.1:p.Tyr806Phe
NM_001382786.1:c.2396A>T NP_001369715.1:p.Tyr799Phe
NM_001382787.1:c.2390A>T NP_001369716.1:p.Tyr797Phe
NM_001382788.1:c.2345A>T NP_001369717.1:p.Tyr782Phe
NM_001382789.1:c.2336A>T NP_001369718.1:p.Tyr779Phe
NM_001382790.1:c.2312A>T NP_001369719.1:p.Tyr771Phe
NM_001382791.1:c.2306A>T NP_001369720.1:p.Tyr769Phe
NM_001382792.1:c.2279A>T NP_001369721.1:p.Tyr760Phe
NM_001382793.1:c.2273A>T NP_001369722.1:p.Tyr758Phe
NM_001382794.1:c.2273A>T NP_001369723.1:p.Tyr758Phe
NM_001382795.1:c.2267A>T NP_001369724.1:p.Tyr756Phe
NM_001382796.1:c.2315A>T NP_001369725.1:p.Tyr772Phe
NM_001382797.1:c.2216A>T NP_001369726.1:p.Tyr739Phe
NM_001382798.1:c.2315A>T NP_001369727.1:p.Tyr772Phe
NM_001382799.1:c.2135A>T NP_001369728.1:p.Tyr712Phe
NM_001382800.1:c.2308-316A>T NP_001369729.1:n.2308-316A>T
NM_001382801.1:c.2267A>T NP_001369730.1:p.Tyr756Phe
NM_001382802.1:c.2057A>T NP_001369731.1:p.Tyr686Phe
NM_001382803.1:c.2273A>T NP_001369732.1:p.Tyr758Phe
NM_001382804.1:c.1487A>T NP_001369733.1:p.Tyr496Phe
NM_001382805.1:c.2208+1073A>T NP_001369734.1:n.2208+1073A>T
NM_001382806.1:c.1277A>T NP_001369735.1:p.Tyr426Phe
NM_004448.4:c.2315A>T MANE Select NP_004439.2:p.Tyr772Phe
NR_110535.2:n.2553A>T