Canonical Allele Identifier: CA343228795

Gene: SLAMF8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159833021C>G , CM000663.2:g.159833021C>G	GRCh38
NC_000001.10:g.159802811C>G , CM000663.1:g.159802811C>G	GRCh37
NC_000001.9:g.158069435C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020125.3:c.513C>G MANE Select	NP_064510.1:p.Asp171Glu
ENST00000289707.10:c.513C>G MANE Select	ENSP00000289707.5:p.Asp171Glu
NM_001330741.1:c.186C>G	NP_001317670.1:p.Asp62Glu
NM_001330741.2:c.186C>G	NP_001317670.1:p.Asp62Glu
NM_020125.2:c.513C>G	NP_064510.1:p.Asp171Glu
ENST00000289707.9:c.513C>G	ENSP00000289707.5:p.Asp171Glu
ENST00000368104.4:c.186C>G	ENSP00000357084.4:p.Asp62Glu
ENST00000471286.5:n.331C>G
ENST00000497141.1:n.17C>G
XM_005245345.2:c.513C>G	XP_005245402.1:p.Asp171Glu
XM_005245345.3:c.513C>G	XP_005245402.1:p.Asp171Glu
XM_011509775.1:c.513C>G	XP_011508077.1:p.Asp171Glu
XM_011509775.2:c.513C>G	XP_011508077.1:p.Asp171Glu
XM_011509776.1:c.495C>G	XP_011508078.1:p.Asp165Glu
XM_011509776.2:c.495C>G	XP_011508078.1:p.Asp165Glu
XM_011509777.1:c.513C>G	XP_011508079.1:p.Asp171Glu
XM_011509777.3:c.513C>G	XP_011508079.1:p.Asp171Glu
XM_011509778.1:c.384C>G	XP_011508080.1:p.Asp128Glu
XM_011509778.2:c.384C>G	XP_011508080.1:p.Asp128Glu
XM_011509779.1:c.186C>G	XP_011508081.1:p.Asp62Glu
XM_011509779.2:c.186C>G	XP_011508081.1:p.Asp62Glu
XM_011509780.1:c.-284C>G	XP_011508082.1:n.-284C>G
XM_017001844.2:c.513C>G	XP_016857333.1:p.Asp171Glu
XM_017001845.2:c.513C>G	XP_016857334.1:p.Asp171Glu
XM_017001846.1:c.495C>G	XP_016857335.1:p.Asp165Glu