Canonical Allele Identifier: CA929737

Gene: BCL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85267836del , CM000663.2:g.85267836del	GRCh38
NC_000001.10:g.85733519del , CM000663.1:g.85733519del	GRCh37
NC_000001.9:g.85506107del	NCBI36
NG_012216.1:g.15071del
NG_012216.2:g.14075del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620248.3:c.466del	ENSP00000480561.2:p.Ser156LeufsTer6
ENST00000620248.2:c.466del	ENSP00000480561.2:p.Ser156LeufsTer6
ENST00000648566.1:c.499del MANE Select	ENSP00000498104.1:p.Ser167LeufsTer6
ENST00000650582.1:n.1030del
ENST00000370580.5:c.499del	ENSP00000359612.1:p.Ser167LeufsTer6
ENST00000620248.1:c.464del
NM_003921.4:c.499del	NP_003912.1:p.Ser167LeufsTer6
XM_005271311.2:c.466del	XP_005271368.1:p.Ser156LeufsTer6
XM_011542397.1:c.658del	XP_011540699.1:p.Ser220LeufsTer6
XM_011542398.1:c.625del	XP_011540700.1:p.Ser209LeufsTer6
XM_011542399.1:c.445del	XP_011540701.1:p.Ser149LeufsTer6
NM_001320715.1:c.466del	NP_001307644.1:p.Ser156LeufsTer6
NM_003921.5:c.499del MANE Select	NP_003912.1:p.Ser167LeufsTer6
XM_011542397.3:c.658del	XP_011540699.1:p.Ser220LeufsTer6
XM_011542398.2:c.625del	XP_011540700.1:p.Ser209LeufsTer6
XM_011542399.2:c.445del	XP_011540701.1:p.Ser149LeufsTer6
NM_001320715.2:c.466del	NP_001307644.1:p.Ser156LeufsTer6