Canonical Allele Identifier: CA1202396866
Gene: SLAMF1 HGNC NCBI

Linked Data

dbSNP Id: rs1659770533

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160624370T>C , CM000663.2:g.160624370T>C GRCh38
NC_000001.10:g.160594160T>C , CM000663.1:g.160594160T>C GRCh37
NC_000001.9:g.158860784T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302035.11:c.701-185A>G MANE Select ENSP00000306190.6:n.701-185A>G
ENST00000235739.6:c.369+12867A>G ENSP00000235739.6:n.369+12867A>G
ENST00000302035.10:c.701-185A>G ENSP00000306190.6:n.701-185A>G
ENST00000538290.2:c.701-185A>G ENSP00000438406.2:n.701-185A>G
NM_003037.3:c.701-185A>G NP_003028.1:n.701-185A>G
NR_104399.1:n.1067-185A>G
NR_104400.1:n.1066+10243A>G
NR_104401.1:n.1062-185A>G
XM_005245456.2:c.701-4521A>G XP_005245513.1:n.701-4521A>G
XM_011509905.1:c.284-185A>G XP_011508207.1:n.284-185A>G
NM_001330754.1:c.701-185A>G NP_001317683.1:n.701-185A>G
NM_003037.4:c.701-185A>G NP_003028.1:n.701-185A>G
NR_104399.2:n.1067-185A>G
NR_104400.2:n.1066+10243A>G
NR_104401.2:n.1062-185A>G
XM_005245456.4:c.701-4521A>G XP_005245513.1:n.701-4521A>G
XM_011509905.3:c.284-185A>G XP_011508207.1:n.284-185A>G
XM_017002130.2:c.701-185A>G XP_016857619.1:n.701-185A>G
XM_017002131.2:c.284-185A>G XP_016857620.1:n.284-185A>G
NR_104399.3:n.800-185A>G
NR_104400.3:n.799+10243A>G
NR_104401.3:n.795-185A>G
NM_001330754.2:c.701-185A>G NP_001317683.1:n.701-185A>G
NM_003037.5:c.701-185A>G MANE Select NP_003028.1:n.701-185A>G