Canonical Allele Identifier: CA2574451904

Gene: BCL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270747del , CM000663.2:g.85270747del	GRCh38
NC_000001.10:g.85736430del , CM000663.1:g.85736430del	GRCh37
NC_000001.9:g.85509018del	NCBI36
NG_012216.1:g.12154del
NG_012216.2:g.11158del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620248.3:c.217del	ENSP00000480561.2:p.Gln73ArgfsTer23
ENST00000620248.2:c.217del	ENSP00000480561.2:p.Gln73ArgfsTer23
ENST00000648566.1:c.217del MANE Select	ENSP00000498104.1:p.Gln73ArgfsTer23
ENST00000649434.1:n.283del
ENST00000650582.1:n.748del
ENST00000370580.5:c.217del	ENSP00000359612.1:p.Gln73ArgfsTer23
ENST00000620248.1:c.217del	ENSP00000480561.1:p.Gln73ArgfsTer23
NM_003921.4:c.217del	NP_003912.1:p.Gln73ArgfsTer23
XM_005271311.2:c.217del	XP_005271368.1:p.Gln73ArgfsTer23
XM_011542397.1:c.376del	XP_011540699.1:p.Gln126ArgfsTer23
XM_011542398.1:c.376del	XP_011540700.1:p.Gln126ArgfsTer23
XM_011542399.1:c.163del	XP_011540701.1:p.Gln55ArgfsTer23
NM_001320715.1:c.217del	NP_001307644.1:p.Gln73ArgfsTer23
NM_003921.5:c.217del MANE Select	NP_003912.1:p.Gln73ArgfsTer23
XM_011542397.3:c.376del	XP_011540699.1:p.Gln126ArgfsTer23
XM_011542398.2:c.376del	XP_011540700.1:p.Gln126ArgfsTer23
XM_011542399.2:c.163del	XP_011540701.1:p.Gln55ArgfsTer23
NM_001320715.2:c.217del	NP_001307644.1:p.Gln73ArgfsTer23