Canonical Allele Identifier: CA929790

Gene: BCL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270701C>T , CM000663.2:g.85270701C>T	GRCh38
NC_000001.10:g.85736384C>T , CM000663.1:g.85736384C>T	GRCh37
NC_000001.9:g.85508972C>T	NCBI36
NG_012216.1:g.12200G>A
NG_012216.2:g.11204G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003921.5:c.263G>A MANE Select	NP_003912.1:p.Arg88Gln
ENST00000648566.1:c.263G>A MANE Select	ENSP00000498104.1:p.Arg88Gln
NM_001320715.1:c.263G>A	NP_001307644.1:p.Arg88Gln
NM_001320715.2:c.263G>A	NP_001307644.1:p.Arg88Gln
NM_003921.4:c.263G>A	NP_003912.1:p.Arg88Gln
ENST00000370580.5:c.263G>A	ENSP00000359612.1:p.Arg88Gln
ENST00000620248.1:c.263G>A	ENSP00000480561.1:p.Arg88Gln
ENST00000620248.2:c.263G>A	ENSP00000480561.2:p.Arg88Gln
ENST00000620248.3:c.263G>A	ENSP00000480561.2:p.Arg88Gln
ENST00000649434.1:n.329G>A
ENST00000650582.1:n.794G>A
XM_005271311.2:c.263G>A	XP_005271368.1:p.Arg88Gln
XM_011542397.1:c.422G>A	XP_011540699.1:p.Arg141Gln
XM_011542397.3:c.422G>A	XP_011540699.1:p.Arg141Gln
XM_011542398.1:c.422G>A	XP_011540700.1:p.Arg141Gln
XM_011542398.2:c.422G>A	XP_011540700.1:p.Arg141Gln
XM_011542399.1:c.209G>A	XP_011540701.1:p.Arg70Gln
XM_011542399.2:c.209G>A	XP_011540701.1:p.Arg70Gln