Canonical Allele Identifier: CA1202396906
Gene: SLAMF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160624480T= , CM000663.2:g.160624480T= GRCh38
NC_000001.10:g.160594270T= , CM000663.1:g.160594270T= GRCh37
NC_000001.9:g.158860894T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302035.11:c.701-295A= MANE Select ENSP00000306190.6:n.701-295A=
ENST00000235739.6:c.369+12757A= ENSP00000235739.6:n.369+12757A=
ENST00000302035.10:c.701-295A= ENSP00000306190.6:n.701-295A=
ENST00000538290.2:c.701-295A= ENSP00000438406.2:n.701-295A=
NM_003037.3:c.701-295A= NP_003028.1:n.701-295A=
NR_104399.1:n.1067-295A=
NR_104400.1:n.1066+10133A=
NR_104401.1:n.1062-295A=
XM_005245456.2:c.701-4631A= XP_005245513.1:n.701-4631A=
XM_011509905.1:c.284-295A= XP_011508207.1:n.284-295A=
NM_001330754.1:c.701-295A= NP_001317683.1:n.701-295A=
NM_003037.4:c.701-295A= NP_003028.1:n.701-295A=
NR_104399.2:n.1067-295A=
NR_104400.2:n.1066+10133A=
NR_104401.2:n.1062-295A=
XM_005245456.4:c.701-4631A= XP_005245513.1:n.701-4631A=
XM_011509905.3:c.284-295A= XP_011508207.1:n.284-295A=
XM_017002130.2:c.701-295A= XP_016857619.1:n.701-295A=
XM_017002131.2:c.284-295A= XP_016857620.1:n.284-295A=
NR_104399.3:n.800-295A=
NR_104400.3:n.799+10133A=
NR_104401.3:n.795-295A=
NM_001330754.2:c.701-295A= NP_001317683.1:n.701-295A=
NM_003037.5:c.701-295A= MANE Select NP_003028.1:n.701-295A=