Canonical Allele Identifier: CA399304134
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145862622

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39725064G>T , CM000679.2:g.39725064G>T GRCh38
NC_000017.10:g.37881317G>T , CM000679.1:g.37881317G>T GRCh37
NC_000017.9:g.35134843G>T NCBI36
NG_007503.1:g.41925G>T , LRG_724:g.41925G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2509G>T MANE Select ENSP00000269571.4:p.Glu837Ter
ENST00000269571.9:c.2509G>T ENSP00000269571.4:p.Glu837Ter
ENST00000406381.6:c.2419G>T ENSP00000385185.2:p.Glu807Ter
ENST00000445658.6:c.1681G>T ENSP00000404047.2:p.Glu561Ter
ENST00000541774.5:c.2464G>T ENSP00000446466.1:p.Glu822Ter
ENST00000578373.5:c.*2299G>T ENSP00000463427.1:n.*2299G>T
ENST00000580074.1:c.615G>T
ENST00000583038.5:n.3643G>T
ENST00000584450.5:c.2509G>T ENSP00000463714.1:p.Glu837Ter
ENST00000584601.5:c.2419G>T ENSP00000462438.1:p.Glu807Ter
NM_001005862.2:c.2419G>T , LRG_724t1:c.2419G>T NP_001005862.1:p.Glu807Ter
NM_001289936.1:c.2464G>T , LRG_724t4:c.2464G>T NP_001276865.1:p.Glu822Ter
NM_001289937.1:c.2509G>T NP_001276866.1:p.Glu837Ter
NM_004448.3:c.2509G>T , LRG_724t2:c.2509G>T NP_004439.2:p.Glu837Ter
NR_110535.1:n.2833G>T
XM_024450641.1:c.2647G>T XP_024306409.1:p.Glu883Ter
XM_024450642.1:c.2602G>T XP_024306410.1:p.Glu868Ter
XM_024450643.1:c.2557G>T XP_024306411.1:p.Glu853Ter
NM_001005862.3:c.2419G>T NP_001005862.1:p.Glu807Ter
NM_001289936.2:c.2464G>T NP_001276865.1:p.Glu822Ter
NM_001289937.2:c.2509G>T NP_001276866.1:p.Glu837Ter
NM_001382782.1:c.2419G>T NP_001369711.1:p.Glu807Ter
NM_001382783.1:c.2419G>T NP_001369712.1:p.Glu807Ter
NM_001382784.1:c.2626G>T NP_001369713.1:p.Glu876Ter
NM_001382785.1:c.2611G>T NP_001369714.1:p.Glu871Ter
NM_001382786.1:c.2590G>T NP_001369715.1:p.Glu864Ter
NM_001382787.1:c.2584G>T NP_001369716.1:p.Glu862Ter
NM_001382788.1:c.2539G>T NP_001369717.1:p.Glu847Ter
NM_001382789.1:c.2530G>T NP_001369718.1:p.Glu844Ter
NM_001382790.1:c.2506G>T NP_001369719.1:p.Glu836Ter
NM_001382791.1:c.2500G>T NP_001369720.1:p.Glu834Ter
NM_001382792.1:c.2473G>T NP_001369721.1:p.Glu825Ter
NM_001382793.1:c.2467G>T NP_001369722.1:p.Glu823Ter
NM_001382794.1:c.2467G>T NP_001369723.1:p.Glu823Ter
NM_001382795.1:c.2461G>T NP_001369724.1:p.Glu821Ter
NM_001382796.1:c.2509G>T NP_001369725.1:p.Glu837Ter
NM_001382797.1:c.2410G>T NP_001369726.1:p.Glu804Ter
NM_001382798.1:c.2493+153G>T NP_001369727.1:n.2493+153G>T
NM_001382799.1:c.2329G>T NP_001369728.1:p.Glu777Ter
NM_001382800.1:c.2323G>T NP_001369729.1:p.Glu775Ter
NM_001382801.1:c.2445+153G>T NP_001369730.1:n.2445+153G>T
NM_001382802.1:c.2251G>T NP_001369731.1:p.Glu751Ter
NM_001382803.1:c.2467G>T NP_001369732.1:p.Glu823Ter
NM_001382804.1:c.1681G>T NP_001369733.1:p.Glu561Ter
NM_001382805.1:c.2208+1404G>T NP_001369734.1:n.2208+1404G>T
NM_001382806.1:c.1471G>T NP_001369735.1:p.Glu491Ter
NM_004448.4:c.2509G>T MANE Select NP_004439.2:p.Glu837Ter
NR_110535.2:n.2747G>T