Canonical Allele Identifier: CA2476011412

Gene: BCL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85267930G= , CM000663.2:g.85267930G=	GRCh38
NC_000001.10:g.85733613G= , CM000663.1:g.85733613G=	GRCh37
NC_000001.9:g.85506201G=	NCBI36
NG_012216.1:g.14971C=
NG_012216.2:g.13975C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620248.3:c.366C=	ENSP00000480561.2:p.Leu122=
ENST00000620248.2:c.366C=	ENSP00000480561.2:p.Leu122=
ENST00000648566.1:c.399C= MANE Select	ENSP00000498104.1:p.Leu133=
ENST00000650582.1:n.930C=
ENST00000370580.5:c.399C=	ENSP00000359612.1:p.Leu133=
ENST00000620248.1:c.366C=	ENSP00000480561.1:p.Leu122=
NM_003921.4:c.399C=	NP_003912.1:p.Leu133=
XM_005271311.2:c.366C=	XP_005271368.1:p.Leu122=
XM_011542397.1:c.558C=	XP_011540699.1:p.Leu186=
XM_011542398.1:c.525C=	XP_011540700.1:p.Leu175=
XM_011542399.1:c.345C=	XP_011540701.1:p.Leu115=
NM_001320715.1:c.366C=	NP_001307644.1:p.Leu122=
NM_003921.5:c.399C= MANE Select	NP_003912.1:p.Leu133=
XM_011542397.3:c.558C=	XP_011540699.1:p.Leu186=
XM_011542398.2:c.525C=	XP_011540700.1:p.Leu175=
XM_011542399.2:c.345C=	XP_011540701.1:p.Leu115=
NM_001320715.2:c.366C=	NP_001307644.1:p.Leu122=