Canonical Allele Identifier: CA129156

Gene: BCL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85267841G>A , CM000663.2:g.85267841G>A	GRCh38
NC_000001.10:g.85733524G>A , CM000663.1:g.85733524G>A	GRCh37
NC_000001.9:g.85506112G>A	NCBI36
NG_012216.1:g.15060C>T
NG_012216.2:g.14064C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003921.5:c.488C>T MANE Select	NP_003912.1:p.Thr163Met
ENST00000648566.1:c.488C>T MANE Select	ENSP00000498104.1:p.Thr163Met
NM_001320715.1:c.455C>T	NP_001307644.1:p.Thr152Met
NM_001320715.2:c.455C>T	NP_001307644.1:p.Thr152Met
NM_003921.4:c.488C>T	NP_003912.1:p.Thr163Met
ENST00000370580.5:c.488C>T	ENSP00000359612.1:p.Thr163Met
ENST00000620248.1:c.455C>T	ENSP00000480561.1:p.Thr152Met
ENST00000620248.2:c.455C>T	ENSP00000480561.2:p.Thr152Met
ENST00000620248.3:c.455C>T	ENSP00000480561.2:p.Thr152Met
ENST00000650582.1:n.1019C>T
XM_005271311.2:c.455C>T	XP_005271368.1:p.Thr152Met
XM_011542397.1:c.647C>T	XP_011540699.1:p.Thr216Met
XM_011542397.3:c.647C>T	XP_011540699.1:p.Thr216Met
XM_011542398.1:c.614C>T	XP_011540700.1:p.Thr205Met
XM_011542398.2:c.614C>T	XP_011540700.1:p.Thr205Met
XM_011542399.1:c.434C>T	XP_011540701.1:p.Thr145Met
XM_011542399.2:c.434C>T	XP_011540701.1:p.Thr145Met