Canonical Allele Identifier: CA1008355477

Gene: SLAMF1

Linked Data

• dbSNP Id: rs1659776625

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160624466T>C , CM000663.2:g.160624466T>C	GRCh38
NC_000001.10:g.160594256T>C , CM000663.1:g.160594256T>C	GRCh37
NC_000001.9:g.158860880T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000302035.11:c.701-281A>G MANE Select	ENSP00000306190.6:n.701-281A>G
ENST00000235739.6:c.369+12771A>G	ENSP00000235739.6:n.369+12771A>G
ENST00000302035.10:c.701-281A>G	ENSP00000306190.6:n.701-281A>G
ENST00000538290.2:c.701-281A>G	ENSP00000438406.2:n.701-281A>G
NM_003037.3:c.701-281A>G	NP_003028.1:n.701-281A>G
NR_104399.1:n.1067-281A>G
NR_104400.1:n.1066+10147A>G
NR_104401.1:n.1062-281A>G
XM_005245456.2:c.701-4617A>G	XP_005245513.1:n.701-4617A>G
XM_011509905.1:c.284-281A>G	XP_011508207.1:n.284-281A>G
NM_001330754.1:c.701-281A>G	NP_001317683.1:n.701-281A>G
NM_003037.4:c.701-281A>G	NP_003028.1:n.701-281A>G
NR_104399.2:n.1067-281A>G
NR_104400.2:n.1066+10147A>G
NR_104401.2:n.1062-281A>G
XM_005245456.4:c.701-4617A>G	XP_005245513.1:n.701-4617A>G
XM_011509905.3:c.284-281A>G	XP_011508207.1:n.284-281A>G
XM_017002130.2:c.701-281A>G	XP_016857619.1:n.701-281A>G
XM_017002131.2:c.284-281A>G	XP_016857620.1:n.284-281A>G
NR_104399.3:n.800-281A>G
NR_104400.3:n.799+10147A>G
NR_104401.3:n.795-281A>G
NM_001330754.2:c.701-281A>G	NP_001317683.1:n.701-281A>G
NM_003037.5:c.701-281A>G MANE Select	NP_003028.1:n.701-281A>G