Canonical Allele Identifier: CA340951918
Gene: BCL10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.85270834T>A , CM000663.2:g.85270834T>A GRCh38
NC_000001.10:g.85736517T>A , CM000663.1:g.85736517T>A GRCh37
NC_000001.9:g.85509105T>A NCBI36
NG_012216.1:g.12067A>T
NG_012216.2:g.11071A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000620248.3:c.130A>T ENSP00000480561.2:p.Lys44Ter
ENST00000620248.2:c.130A>T ENSP00000480561.2:p.Lys44Ter
ENST00000648566.1:c.130A>T MANE Select ENSP00000498104.1:p.Lys44Ter
ENST00000649060.1:c.*1239A>T ENSP00000497490.1:n.*1239A>T
ENST00000649434.1:n.196A>T
ENST00000650582.1:n.661A>T
ENST00000370580.5:c.130A>T ENSP00000359612.1:p.Lys44Ter
ENST00000620248.1:c.130A>T ENSP00000480561.1:p.Lys44Ter
NM_003921.4:c.130A>T NP_003912.1:p.Lys44Ter
XM_005271311.2:c.130A>T XP_005271368.1:p.Lys44Ter
XM_011542397.1:c.289A>T XP_011540699.1:p.Lys97Ter
XM_011542398.1:c.289A>T XP_011540700.1:p.Lys97Ter
XM_011542399.1:c.76A>T XP_011540701.1:p.Lys26Ter
NM_001320715.1:c.130A>T NP_001307644.1:p.Lys44Ter
NM_003921.5:c.130A>T MANE Select NP_003912.1:p.Lys44Ter
XM_011542397.3:c.289A>T XP_011540699.1:p.Lys97Ter
XM_011542398.2:c.289A>T XP_011540700.1:p.Lys97Ter
XM_011542399.2:c.76A>T XP_011540701.1:p.Lys26Ter
NM_001320715.2:c.130A>T NP_001307644.1:p.Lys44Ter