Canonical Allele Identifier: CA2476012514

Gene: BCL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270640A= , CM000663.2:g.85270640A=	GRCh38
NC_000001.10:g.85736323A= , CM000663.1:g.85736323A=	GRCh37
NC_000001.9:g.85508911A=	NCBI36
NG_012216.1:g.12261T=
NG_012216.2:g.11265T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000620248.3:c.324T=	ENSP00000480561.2:p.Asn108=
ENST00000620248.2:c.324T=	ENSP00000480561.2:p.Asn108=
ENST00000648566.1:c.324T= MANE Select	ENSP00000498104.1:p.Asn108=
ENST00000649434.1:n.390T=
ENST00000650582.1:n.855T=
ENST00000370580.5:c.324T=	ENSP00000359612.1:p.Asn108=
ENST00000620248.1:c.324T=	ENSP00000480561.1:p.Asn108=
NM_003921.4:c.324T=	NP_003912.1:p.Asn108=
XM_005271311.2:c.324T=	XP_005271368.1:p.Asn108=
XM_011542397.1:c.483T=	XP_011540699.1:p.Asn161=
XM_011542398.1:c.483T=	XP_011540700.1:p.Asn161=
XM_011542399.1:c.270T=	XP_011540701.1:p.Asn90=
NM_001320715.1:c.324T=	NP_001307644.1:p.Asn108=
NM_003921.5:c.324T= MANE Select	NP_003912.1:p.Asn108=
XM_011542397.3:c.483T=	XP_011540699.1:p.Asn161=
XM_011542398.2:c.483T=	XP_011540700.1:p.Asn161=
XM_011542399.2:c.270T=	XP_011540701.1:p.Asn90=
NM_001320715.2:c.324T=	NP_001307644.1:p.Asn108=