Canonical Allele Identifier: CA2476012570

Gene: BCL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270832T= , CM000663.2:g.85270832T=	GRCh38
NC_000001.10:g.85736515T= , CM000663.1:g.85736515T=	GRCh37
NC_000001.9:g.85509103T=	NCBI36
NG_012216.1:g.12069A=
NG_012216.2:g.11073A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620248.3:c.132A=	ENSP00000480561.2:p.Lys44=
ENST00000620248.2:c.132A=	ENSP00000480561.2:p.Lys44=
ENST00000648566.1:c.132A= MANE Select	ENSP00000498104.1:p.Lys44=
ENST00000649060.1:c.*1241A=	ENSP00000497490.1:n.*1241A=
ENST00000649434.1:n.198A=
ENST00000650582.1:n.663A=
ENST00000370580.5:c.132A=	ENSP00000359612.1:p.Lys44=
ENST00000620248.1:c.132A=	ENSP00000480561.1:p.Lys44=
NM_003921.4:c.132A=	NP_003912.1:p.Lys44=
XM_005271311.2:c.132A=	XP_005271368.1:p.Lys44=
XM_011542397.1:c.291A=	XP_011540699.1:p.Lys97=
XM_011542398.1:c.291A=	XP_011540700.1:p.Lys97=
XM_011542399.1:c.78A=	XP_011540701.1:p.Lys26=
NM_001320715.1:c.132A=	NP_001307644.1:p.Lys44=
NM_003921.5:c.132A= MANE Select	NP_003912.1:p.Lys44=
XM_011542397.3:c.291A=	XP_011540699.1:p.Lys97=
XM_011542398.2:c.291A=	XP_011540700.1:p.Lys97=
XM_011542399.2:c.78A=	XP_011540701.1:p.Lys26=
NM_001320715.2:c.132A=	NP_001307644.1:p.Lys44=