Canonical Allele Identifier: CA2476012571

Gene: BCL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270839C= , CM000663.2:g.85270839C=	GRCh38
NC_000001.10:g.85736522C= , CM000663.1:g.85736522C=	GRCh37
NC_000001.9:g.85509110C=	NCBI36
NG_012216.1:g.12062G=
NG_012216.2:g.11066G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620248.3:c.125G=	ENSP00000480561.2:p.Arg42=
ENST00000620248.2:c.125G=	ENSP00000480561.2:p.Arg42=
ENST00000648566.1:c.125G= MANE Select	ENSP00000498104.1:p.Arg42=
ENST00000649060.1:c.*1234G=	ENSP00000497490.1:n.*1234G=
ENST00000649434.1:n.191G=
ENST00000650582.1:n.656G=
ENST00000370580.5:c.125G=	ENSP00000359612.1:p.Arg42=
ENST00000620248.1:c.125G=	ENSP00000480561.1:p.Arg42=
NM_003921.4:c.125G=	NP_003912.1:p.Arg42=
XM_005271311.2:c.125G=	XP_005271368.1:p.Arg42=
XM_011542397.1:c.284G=	XP_011540699.1:p.Arg95=
XM_011542398.1:c.284G=	XP_011540700.1:p.Arg95=
XM_011542399.1:c.71G=	XP_011540701.1:p.Arg24=
NM_001320715.1:c.125G=	NP_001307644.1:p.Arg42=
NM_003921.5:c.125G= MANE Select	NP_003912.1:p.Arg42=
XM_011542397.3:c.284G=	XP_011540699.1:p.Arg95=
XM_011542398.2:c.284G=	XP_011540700.1:p.Arg95=
XM_011542399.2:c.71G=	XP_011540701.1:p.Arg24=
NM_001320715.2:c.125G=	NP_001307644.1:p.Arg42=