Canonical Allele Identifier: CA399303295
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145850754

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724820T>A , CM000679.2:g.39724820T>A GRCh38
NC_000017.10:g.37881073T>A , CM000679.1:g.37881073T>A GRCh37
NC_000017.9:g.35134599T>A NCBI36
NG_007503.1:g.41681T>A , LRG_724:g.41681T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2402T>A MANE Select ENSP00000269571.4:p.Met801Lys
ENST00000269571.9:c.2402T>A ENSP00000269571.4:p.Met801Lys
ENST00000406381.6:c.2312T>A ENSP00000385185.2:p.Met771Lys
ENST00000445658.6:c.1574T>A ENSP00000404047.2:p.Met525Lys
ENST00000541774.5:c.2357T>A ENSP00000446466.1:p.Met786Lys
ENST00000578373.5:c.*2192T>A ENSP00000463427.1:n.*2192T>A
ENST00000580074.1:c.508T>A
ENST00000583038.5:n.3536T>A
ENST00000584450.5:c.2402T>A ENSP00000463714.1:p.Met801Lys
ENST00000584601.5:c.2312T>A ENSP00000462438.1:p.Met771Lys
NM_001005862.2:c.2312T>A , LRG_724t1:c.2312T>A NP_001005862.1:p.Met771Lys
NM_001289936.1:c.2357T>A , LRG_724t4:c.2357T>A NP_001276865.1:p.Met786Lys
NM_001289937.1:c.2402T>A NP_001276866.1:p.Met801Lys
NM_004448.3:c.2402T>A , LRG_724t2:c.2402T>A NP_004439.2:p.Met801Lys
NR_110535.1:n.2726T>A
XM_024450641.1:c.2540T>A XP_024306409.1:p.Met847Lys
XM_024450642.1:c.2495T>A XP_024306410.1:p.Met832Lys
XM_024450643.1:c.2450T>A XP_024306411.1:p.Met817Lys
NM_001005862.3:c.2312T>A NP_001005862.1:p.Met771Lys
NM_001289936.2:c.2357T>A NP_001276865.1:p.Met786Lys
NM_001289937.2:c.2402T>A NP_001276866.1:p.Met801Lys
NM_001382782.1:c.2312T>A NP_001369711.1:p.Met771Lys
NM_001382783.1:c.2312T>A NP_001369712.1:p.Met771Lys
NM_001382784.1:c.2519T>A NP_001369713.1:p.Met840Lys
NM_001382785.1:c.2504T>A NP_001369714.1:p.Met835Lys
NM_001382786.1:c.2483T>A NP_001369715.1:p.Met828Lys
NM_001382787.1:c.2477T>A NP_001369716.1:p.Met826Lys
NM_001382788.1:c.2432T>A NP_001369717.1:p.Met811Lys
NM_001382789.1:c.2423T>A NP_001369718.1:p.Met808Lys
NM_001382790.1:c.2399T>A NP_001369719.1:p.Met800Lys
NM_001382791.1:c.2393T>A NP_001369720.1:p.Met798Lys
NM_001382792.1:c.2366T>A NP_001369721.1:p.Met789Lys
NM_001382793.1:c.2360T>A NP_001369722.1:p.Met787Lys
NM_001382794.1:c.2360T>A NP_001369723.1:p.Met787Lys
NM_001382795.1:c.2354T>A NP_001369724.1:p.Met785Lys
NM_001382796.1:c.2402T>A NP_001369725.1:p.Met801Lys
NM_001382797.1:c.2303T>A NP_001369726.1:p.Met768Lys
NM_001382798.1:c.2402T>A NP_001369727.1:p.Met801Lys
NM_001382799.1:c.2222T>A NP_001369728.1:p.Met741Lys
NM_001382800.1:c.2308-229T>A NP_001369729.1:n.2308-229T>A
NM_001382801.1:c.2354T>A NP_001369730.1:p.Met785Lys
NM_001382802.1:c.2144T>A NP_001369731.1:p.Met715Lys
NM_001382803.1:c.2360T>A NP_001369732.1:p.Met787Lys
NM_001382804.1:c.1574T>A NP_001369733.1:p.Met525Lys
NM_001382805.1:c.2208+1160T>A NP_001369734.1:n.2208+1160T>A
NM_001382806.1:c.1364T>A NP_001369735.1:p.Met455Lys
NM_004448.4:c.2402T>A MANE Select NP_004439.2:p.Met801Lys
NR_110535.2:n.2640T>A