Canonical Allele Identifier: CA3081385406

Gene: SLAMF7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160752967C= , CM000663.2:g.160752967C=	GRCh38
NC_000001.10:g.160722757C= , CM000663.1:g.160722757C=	GRCh37
NC_000001.9:g.158989381C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021181.5:c.937-139C= MANE Select	NP_067004.3:n.937-139C=
ENST00000368043.8:c.937-139C= MANE Select	ENSP00000357022.3:n.937-139C=
NM_001282588.1:c.440-139C=	NP_001269517.1:n.440-139C=
NM_001282588.2:c.440-139C=	NP_001269517.1:n.440-139C=
NM_001282589.1:c.544-139C=	NP_001269518.1:n.544-139C=
NM_001282589.2:c.544-139C=	NP_001269518.1:n.544-139C=
NM_001282590.1:c.616-139C=	NP_001269519.1:n.616-139C=
NM_001282590.2:c.616-139C=	NP_001269519.1:n.616-139C=
NM_001282591.1:c.496-139C=	NP_001269520.1:n.496-139C=
NM_001282591.2:c.496-139C=	NP_001269520.1:n.496-139C=
NM_001282592.1:c.833-139C=	NP_001269521.1:n.833-139C=
NM_001282592.2:c.833-139C=	NP_001269521.1:n.833-139C=
NM_001282593.1:c.392-139C=	NP_001269522.1:n.392-139C=
NM_001282593.2:c.392-139C=	NP_001269522.1:n.392-139C=
NM_001282594.1:c.655-139C=	NP_001269523.1:n.655-139C=
NM_001282594.2:c.655-139C=	NP_001269523.1:n.655-139C=
NM_001282595.1:c.535-139C=	NP_001269524.1:n.535-139C=
NM_001282596.1:c.512-139C=	NP_001269525.1:n.512-139C=
NM_001282596.2:c.512-139C=	NP_001269525.1:n.512-139C=
NM_021181.4:c.937-139C=	NP_067004.3:n.937-139C=
ENST00000359331.8:c.833-139C=	ENSP00000352281.4:n.833-139C=
ENST00000368042.7:c.616-139C=	ENSP00000357021.3:n.616-139C=
ENST00000368043.7:c.937-139C=	ENSP00000357022.3:n.937-139C=
ENST00000441662.6:c.544-139C=	ENSP00000405605.2:n.544-139C=
ENST00000444090.6:c.440-139C=	ENSP00000416592.2:n.440-139C=
ENST00000458104.6:c.392-139C=	ENSP00000403294.2:n.392-139C=
ENST00000458602.6:c.496-139C=	ENSP00000409965.2:n.496-139C=
ENST00000484221.1:n.1827-139C=
ENST00000621377.4:c.655-139C=	ENSP00000483774.1:n.655-139C=
XM_005245386.1:c.817-139C=	XP_005245443.1:n.817-139C=
XM_006711471.1:c.713-139C=	XP_006711534.1:n.713-139C=
XM_011509828.1:c.976-139C=	XP_011508130.1:n.976-139C=
XM_011509829.1:c.872-139C=	XP_011508131.1:n.872-139C=
XM_024448757.1:c.1147-139C=	XP_024304525.1:n.1147-139C=