Canonical Allele Identifier: CA399303845
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145853631

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724892G>T , CM000679.2:g.39724892G>T GRCh38
NC_000017.10:g.37881145G>T , CM000679.1:g.37881145G>T GRCh37
NC_000017.9:g.35134671G>T NCBI36
NG_007503.1:g.41753G>T , LRG_724:g.41753G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2474G>T MANE Select ENSP00000269571.4:p.Trp825Leu
ENST00000269571.9:c.2474G>T ENSP00000269571.4:p.Trp825Leu
ENST00000406381.6:c.2384G>T ENSP00000385185.2:p.Trp795Leu
ENST00000445658.6:c.1646G>T ENSP00000404047.2:p.Trp549Leu
ENST00000541774.5:c.2429G>T ENSP00000446466.1:p.Trp810Leu
ENST00000578373.5:c.*2264G>T ENSP00000463427.1:n.*2264G>T
ENST00000580074.1:c.580G>T
ENST00000583038.5:n.3608G>T
ENST00000584450.5:c.2474G>T ENSP00000463714.1:p.Trp825Leu
ENST00000584601.5:c.2384G>T ENSP00000462438.1:p.Trp795Leu
NM_001005862.2:c.2384G>T , LRG_724t1:c.2384G>T NP_001005862.1:p.Trp795Leu
NM_001289936.1:c.2429G>T , LRG_724t4:c.2429G>T NP_001276865.1:p.Trp810Leu
NM_001289937.1:c.2474G>T NP_001276866.1:p.Trp825Leu
NM_004448.3:c.2474G>T , LRG_724t2:c.2474G>T NP_004439.2:p.Trp825Leu
NR_110535.1:n.2798G>T
XM_024450641.1:c.2612G>T XP_024306409.1:p.Trp871Leu
XM_024450642.1:c.2567G>T XP_024306410.1:p.Trp856Leu
XM_024450643.1:c.2522G>T XP_024306411.1:p.Trp841Leu
NM_001005862.3:c.2384G>T NP_001005862.1:p.Trp795Leu
NM_001289936.2:c.2429G>T NP_001276865.1:p.Trp810Leu
NM_001289937.2:c.2474G>T NP_001276866.1:p.Trp825Leu
NM_001382782.1:c.2384G>T NP_001369711.1:p.Trp795Leu
NM_001382783.1:c.2384G>T NP_001369712.1:p.Trp795Leu
NM_001382784.1:c.2591G>T NP_001369713.1:p.Trp864Leu
NM_001382785.1:c.2576G>T NP_001369714.1:p.Trp859Leu
NM_001382786.1:c.2555G>T NP_001369715.1:p.Trp852Leu
NM_001382787.1:c.2549G>T NP_001369716.1:p.Trp850Leu
NM_001382788.1:c.2504G>T NP_001369717.1:p.Trp835Leu
NM_001382789.1:c.2495G>T NP_001369718.1:p.Trp832Leu
NM_001382790.1:c.2471G>T NP_001369719.1:p.Trp824Leu
NM_001382791.1:c.2465G>T NP_001369720.1:p.Trp822Leu
NM_001382792.1:c.2438G>T NP_001369721.1:p.Trp813Leu
NM_001382793.1:c.2432G>T NP_001369722.1:p.Trp811Leu
NM_001382794.1:c.2432G>T NP_001369723.1:p.Trp811Leu
NM_001382795.1:c.2426G>T NP_001369724.1:p.Trp809Leu
NM_001382796.1:c.2474G>T NP_001369725.1:p.Trp825Leu
NM_001382797.1:c.2375G>T NP_001369726.1:p.Trp792Leu
NM_001382798.1:c.2474G>T NP_001369727.1:p.Trp825Leu
NM_001382799.1:c.2294G>T NP_001369728.1:p.Trp765Leu
NM_001382800.1:c.2308-157G>T NP_001369729.1:n.2308-157G>T
NM_001382801.1:c.2426G>T NP_001369730.1:p.Trp809Leu
NM_001382802.1:c.2216G>T NP_001369731.1:p.Trp739Leu
NM_001382803.1:c.2432G>T NP_001369732.1:p.Trp811Leu
NM_001382804.1:c.1646G>T NP_001369733.1:p.Trp549Leu
NM_001382805.1:c.2208+1232G>T NP_001369734.1:n.2208+1232G>T
NM_001382806.1:c.1436G>T NP_001369735.1:p.Trp479Leu
NM_004448.4:c.2474G>T MANE Select NP_004439.2:p.Trp825Leu
NR_110535.2:n.2712G>T