Canonical Allele Identifier: CA418704461
Gene: BCL10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.85270829_85270830insA , CM000663.2:g.85270829_85270830insA GRCh38
NC_000001.10:g.85736512_85736513insA , CM000663.1:g.85736512_85736513insA GRCh37
NC_000001.9:g.85509100_85509101insA NCBI36
NG_012216.1:g.12071_12072insT
NG_012216.2:g.11075_11076insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000620248.3:c.134_135insT ENSP00000480561.2:p.Lys45AsnfsTer5
ENST00000620248.2:c.134_135insT ENSP00000480561.2:p.Lys45AsnfsTer5
ENST00000648566.1:c.134_135insT MANE Select ENSP00000498104.1:p.Lys45AsnfsTer5
ENST00000649060.1:c.*1243_*1244insT ENSP00000497490.1:n.*1243_*1244insT
ENST00000649434.1:n.200_201insT
ENST00000650582.1:n.665_666insT
ENST00000370580.5:c.134_135insT ENSP00000359612.1:p.Lys45AsnfsTer5
ENST00000620248.1:c.134_135insT ENSP00000480561.1:p.Lys45AsnfsTer5
NM_003921.4:c.134_135insT NP_003912.1:p.Lys45AsnfsTer5
XM_005271311.2:c.134_135insT XP_005271368.1:p.Lys45AsnfsTer5
XM_011542397.1:c.293_294insT XP_011540699.1:p.Lys98AsnfsTer5
XM_011542398.1:c.293_294insT XP_011540700.1:p.Lys98AsnfsTer5
XM_011542399.1:c.80_81insT XP_011540701.1:p.Lys27AsnfsTer5
NM_001320715.1:c.134_135insT NP_001307644.1:p.Lys45AsnfsTer5
NM_003921.5:c.134_135insT MANE Select NP_003912.1:p.Lys45AsnfsTer5
XM_011542397.3:c.293_294insT XP_011540699.1:p.Lys98AsnfsTer5
XM_011542398.2:c.293_294insT XP_011540700.1:p.Lys98AsnfsTer5
XM_011542399.2:c.80_81insT XP_011540701.1:p.Lys27AsnfsTer5
NM_001320715.2:c.134_135insT NP_001307644.1:p.Lys45AsnfsTer5