Canonical Allele Identifier: CA399281657
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145558007

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39711928A>T , CM000679.2:g.39711928A>T GRCh38
NC_000017.10:g.37868181A>T , CM000679.1:g.37868181A>T GRCh37
NC_000017.9:g.35121707A>T NCBI36
NG_007503.1:g.28789A>T , LRG_724:g.28789A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.902A>T MANE Select ENSP00000269571.4:p.Tyr301Phe
ENST00000269571.9:c.902A>T ENSP00000269571.4:p.Tyr301Phe
ENST00000406381.6:c.812A>T ENSP00000385185.2:p.Tyr271Phe
ENST00000445658.6:c.74A>T ENSP00000404047.2:p.Asp25Val
ENST00000541774.5:c.857A>T ENSP00000446466.1:p.Tyr286Phe
ENST00000578199.5:c.812A>T ENSP00000462808.1:p.Tyr271Phe
ENST00000578373.5:c.*692A>T ENSP00000463427.1:n.*692A>T
ENST00000578502.1:c.127A>T
ENST00000582648.5:c.226A>T ENSP00000462024.1:p.Thr76Ser
ENST00000582788.5:n.391A>T
ENST00000583038.5:n.1594A>T
ENST00000584450.5:c.902A>T ENSP00000463714.1:p.Tyr301Phe
ENST00000584601.5:c.812A>T ENSP00000462438.1:p.Tyr271Phe
ENST00000584908.5:n.914A>T
NM_001005862.2:c.812A>T , LRG_724t1:c.812A>T NP_001005862.1:p.Tyr271Phe
NM_001289936.1:c.857A>T , LRG_724t4:c.857A>T NP_001276865.1:p.Tyr286Phe
NM_001289937.1:c.902A>T NP_001276866.1:p.Tyr301Phe
NM_001289938.1:c.812A>T , LRG_724t3:c.812A>T NP_001276867.1:p.Tyr271Phe
NM_004448.3:c.902A>T , LRG_724t2:c.902A>T NP_004439.2:p.Tyr301Phe
NR_110535.1:n.1226A>T
XM_024450641.1:c.1040A>T XP_024306409.1:p.Tyr347Phe
XM_024450642.1:c.995A>T XP_024306410.1:p.Tyr332Phe
XM_024450643.1:c.950A>T XP_024306411.1:p.Tyr317Phe
NM_001005862.3:c.812A>T NP_001005862.1:p.Tyr271Phe
NM_001289936.2:c.857A>T NP_001276865.1:p.Tyr286Phe
NM_001289937.2:c.902A>T NP_001276866.1:p.Tyr301Phe
NM_001289938.2:c.812A>T NP_001276867.1:p.Tyr271Phe
NM_001382782.1:c.812A>T NP_001369711.1:p.Tyr271Phe
NM_001382783.1:c.812A>T NP_001369712.1:p.Tyr271Phe
NM_001382784.1:c.902A>T NP_001369713.1:p.Tyr301Phe
NM_001382785.1:c.902A>T NP_001369714.1:p.Tyr301Phe
NM_001382786.1:c.902A>T NP_001369715.1:p.Tyr301Phe
NM_001382787.1:c.977A>T NP_001369716.1:p.Tyr326Phe
NM_001382788.1:c.902A>T NP_001369717.1:p.Tyr301Phe
NM_001382789.1:c.902A>T NP_001369718.1:p.Tyr301Phe
NM_001382790.1:c.902A>T NP_001369719.1:p.Tyr301Phe
NM_001382791.1:c.893A>T NP_001369720.1:p.Tyr298Phe
NM_001382792.1:c.902A>T NP_001369721.1:p.Tyr301Phe
NM_001382793.1:c.902A>T NP_001369722.1:p.Tyr301Phe
NM_001382794.1:c.902A>T NP_001369723.1:p.Tyr301Phe
NM_001382795.1:c.902A>T NP_001369724.1:p.Tyr301Phe
NM_001382796.1:c.902A>T NP_001369725.1:p.Tyr301Phe
NM_001382797.1:c.902A>T NP_001369726.1:p.Tyr301Phe
NM_001382798.1:c.902A>T NP_001369727.1:p.Tyr301Phe
NM_001382799.1:c.722A>T NP_001369728.1:p.Tyr241Phe
NM_001382800.1:c.902A>T NP_001369729.1:p.Tyr301Phe
NM_001382801.1:c.902A>T NP_001369730.1:p.Tyr301Phe
NM_001382802.1:c.644A>T NP_001369731.1:p.His215Leu
NM_001382803.1:c.902A>T NP_001369732.1:p.Tyr301Phe
NM_001382804.1:c.74A>T NP_001369733.1:p.Asp25Val
NM_001382805.1:c.902A>T NP_001369734.1:p.Tyr301Phe
NM_001382806.1:c.902A>T NP_001369735.1:p.Tyr301Phe
NM_004448.4:c.902A>T MANE Select NP_004439.2:p.Tyr301Phe
NR_110535.2:n.1140A>T