Canonical Allele Identifier: CA1139775905

Gene: SLAMF1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160634683G= , CM000663.2:g.160634683G=	GRCh38
NC_000001.10:g.160604473G= , CM000663.1:g.160604473G=	GRCh37
NC_000001.9:g.158871097G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302035.11:c.630C= MANE Select	ENSP00000306190.6:p.Thr210=
ENST00000235739.6:c.369+2554C=	ENSP00000235739.6:n.369+2554C=
ENST00000302035.10:c.630C=	ENSP00000306190.6:p.Thr210=
ENST00000538290.2:c.630C=	ENSP00000438406.2:p.Thr210=
NM_003037.3:c.630C=	NP_003028.1:p.Thr210=
NR_104399.1:n.996C=
NR_104400.1:n.996C=
NR_104401.1:n.991C=
XM_005245456.2:c.630C=	XP_005245513.1:p.Thr210=
XM_005245457.2:c.630C=	XP_005245514.1:p.Thr210=
XM_011509905.1:c.213C=	XP_011508207.1:p.Thr71=
NM_001330754.1:c.630C=	NP_001317683.1:p.Thr210=
NM_003037.4:c.630C=	NP_003028.1:p.Thr210=
NR_104399.2:n.996C=
NR_104400.2:n.996C=
NR_104401.2:n.991C=
XM_005245456.4:c.630C=	XP_005245513.1:p.Thr210=
XM_011509905.3:c.213C=	XP_011508207.1:p.Thr71=
XM_017002130.2:c.630C=	XP_016857619.1:p.Thr210=
XM_017002131.2:c.213C=	XP_016857620.1:p.Thr71=
NR_104399.3:n.729C=
NR_104400.3:n.729C=
NR_104401.3:n.724C=
NM_001330754.2:c.630C=	NP_001317683.1:p.Thr210=
NM_003037.5:c.630C= MANE Select	NP_003028.1:p.Thr210=