Canonical Allele Identifier: CA340951508
Gene: BCL10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.85270734T>A , CM000663.2:g.85270734T>A GRCh38
NC_000001.10:g.85736417T>A , CM000663.1:g.85736417T>A GRCh37
NC_000001.9:g.85509005T>A NCBI36
NG_012216.1:g.12167A>T
NG_012216.2:g.11171A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000620248.3:c.230A>T ENSP00000480561.2:p.Lys77Ile
ENST00000620248.2:c.230A>T ENSP00000480561.2:p.Lys77Ile
ENST00000648566.1:c.230A>T MANE Select ENSP00000498104.1:p.Lys77Ile
ENST00000649434.1:n.296A>T
ENST00000650582.1:n.761A>T
ENST00000370580.5:c.230A>T ENSP00000359612.1:p.Lys77Ile
ENST00000620248.1:c.230A>T ENSP00000480561.1:p.Lys77Ile
NM_003921.4:c.230A>T NP_003912.1:p.Lys77Ile
XM_005271311.2:c.230A>T XP_005271368.1:p.Lys77Ile
XM_011542397.1:c.389A>T XP_011540699.1:p.Lys130Ile
XM_011542398.1:c.389A>T XP_011540700.1:p.Lys130Ile
XM_011542399.1:c.176A>T XP_011540701.1:p.Lys59Ile
NM_001320715.1:c.230A>T NP_001307644.1:p.Lys77Ile
NM_003921.5:c.230A>T MANE Select NP_003912.1:p.Lys77Ile
XM_011542397.3:c.389A>T XP_011540699.1:p.Lys130Ile
XM_011542398.2:c.389A>T XP_011540700.1:p.Lys130Ile
XM_011542399.2:c.176A>T XP_011540701.1:p.Lys59Ile
NM_001320715.2:c.230A>T NP_001307644.1:p.Lys77Ile