Canonical Allele Identifier: CA399314452
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2143313841

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727949C>A , CM000679.2:g.39727949C>A GRCh38
NC_000017.10:g.37884202C>A , CM000679.1:g.37884202C>A GRCh37
NC_000017.9:g.35137728C>A NCBI36
NG_007503.1:g.44810C>A , LRG_724:g.44810C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3673C>A MANE Select ENSP00000269571.4:p.Gln1225Lys
ENST00000269571.9:c.3673C>A ENSP00000269571.4:p.Gln1225Lys
ENST00000406381.6:c.3583C>A ENSP00000385185.2:p.Gln1195Lys
ENST00000445658.6:c.2845C>A ENSP00000404047.2:p.Gln949Lys
ENST00000541774.5:c.3628C>A ENSP00000446466.1:p.Gln1210Lys
ENST00000578373.5:c.*3463C>A ENSP00000463427.1:n.*3463C>A
ENST00000584450.5:c.*252C>A ENSP00000463714.1:n.*252C>A
ENST00000584601.5:c.3583C>A ENSP00000462438.1:p.Gln1195Lys
NM_001005862.2:c.3583C>A , LRG_724t1:c.3583C>A NP_001005862.1:p.Gln1195Lys
NM_001289936.1:c.3628C>A , LRG_724t4:c.3628C>A NP_001276865.1:p.Gln1210Lys
NM_001289937.1:c.*252C>A NP_001276866.1:n.*252C>A
NM_004448.3:c.3673C>A , LRG_724t2:c.3673C>A NP_004439.2:p.Gln1225Lys
NR_110535.1:n.3997C>A
XM_024450641.1:c.3811C>A XP_024306409.1:p.Gln1271Lys
XM_024450642.1:c.3766C>A XP_024306410.1:p.Gln1256Lys
XM_024450643.1:c.3721C>A XP_024306411.1:p.Gln1241Lys
NM_001005862.3:c.3583C>A NP_001005862.1:p.Gln1195Lys
NM_001289936.2:c.3628C>A NP_001276865.1:p.Gln1210Lys
NM_001289937.2:c.*252C>A NP_001276866.1:n.*252C>A
NM_001382782.1:c.3583C>A NP_001369711.1:p.Gln1195Lys
NM_001382783.1:c.3583C>A NP_001369712.1:p.Gln1195Lys
NM_001382784.1:c.3790C>A NP_001369713.1:p.Gln1264Lys
NM_001382785.1:c.3775C>A NP_001369714.1:p.Gln1259Lys
NM_001382786.1:c.3754C>A NP_001369715.1:p.Gln1252Lys
NM_001382787.1:c.3748C>A NP_001369716.1:p.Gln1250Lys
NM_001382788.1:c.3703C>A NP_001369717.1:p.Gln1235Lys
NM_001382789.1:c.3694C>A NP_001369718.1:p.Gln1232Lys
NM_001382790.1:c.3670C>A NP_001369719.1:p.Gln1224Lys
NM_001382791.1:c.3664C>A NP_001369720.1:p.Gln1222Lys
NM_001382792.1:c.3637C>A NP_001369721.1:p.Gln1213Lys
NM_001382793.1:c.3631C>A NP_001369722.1:p.Gln1211Lys
NM_001382794.1:c.3631C>A NP_001369723.1:p.Gln1211Lys
NM_001382795.1:c.3625C>A NP_001369724.1:p.Gln1209Lys
NM_001382796.1:c.3586C>A NP_001369725.1:p.Gln1196Lys
NM_001382797.1:c.3574C>A NP_001369726.1:p.Gln1192Lys
NM_001382798.1:c.3517C>A NP_001369727.1:p.Gln1173Lys
NM_001382799.1:c.3493C>A NP_001369728.1:p.Gln1165Lys
NM_001382800.1:c.3487C>A NP_001369729.1:p.Gln1163Lys
NM_001382801.1:c.3469C>A NP_001369730.1:p.Gln1157Lys
NM_001382802.1:c.3415C>A NP_001369731.1:p.Gln1139Lys
NM_001382803.1:c.*252C>A NP_001369732.1:n.*252C>A
NM_001382804.1:c.2845C>A NP_001369733.1:p.Gln949Lys
NM_001382805.1:c.2722C>A NP_001369734.1:p.Gln908Lys
NM_001382806.1:c.2635C>A NP_001369735.1:p.Gln879Lys
NM_004448.4:c.3673C>A MANE Select NP_004439.2:p.Gln1225Lys
NR_110535.2:n.3911C>A