Canonical Allele Identifier: CA1008364607

Gene: SLAMF7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160752972_160752973del , CM000663.2:g.160752972_160752973del	GRCh38
NC_000001.10:g.160722762_160722763del , CM000663.1:g.160722762_160722763del	GRCh37
NC_000001.9:g.158989386_158989387del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021181.5:c.937-134_937-133del MANE Select	NP_067004.3:n.937-134_937-133del
ENST00000368043.8:c.937-134_937-133del MANE Select	ENSP00000357022.3:n.937-134_937-133del
NM_001282588.1:c.440-134_440-133del	NP_001269517.1:n.440-134_440-133del
NM_001282588.2:c.440-134_440-133del	NP_001269517.1:n.440-134_440-133del
NM_001282589.1:c.544-134_544-133del	NP_001269518.1:n.544-134_544-133del
NM_001282589.2:c.544-134_544-133del	NP_001269518.1:n.544-134_544-133del
NM_001282590.1:c.616-134_616-133del	NP_001269519.1:n.616-134_616-133del
NM_001282590.2:c.616-134_616-133del	NP_001269519.1:n.616-134_616-133del
NM_001282591.1:c.496-134_496-133del	NP_001269520.1:n.496-134_496-133del
NM_001282591.2:c.496-134_496-133del	NP_001269520.1:n.496-134_496-133del
NM_001282592.1:c.833-134_833-133del	NP_001269521.1:n.833-134_833-133del
NM_001282592.2:c.833-134_833-133del	NP_001269521.1:n.833-134_833-133del
NM_001282593.1:c.392-134_392-133del	NP_001269522.1:n.392-134_392-133del
NM_001282593.2:c.392-134_392-133del	NP_001269522.1:n.392-134_392-133del
NM_001282594.1:c.655-134_655-133del	NP_001269523.1:n.655-134_655-133del
NM_001282594.2:c.655-134_655-133del	NP_001269523.1:n.655-134_655-133del
NM_001282595.1:c.535-134_535-133del	NP_001269524.1:n.535-134_535-133del
NM_001282596.1:c.512-134_512-133del	NP_001269525.1:n.512-134_512-133del
NM_001282596.2:c.512-134_512-133del	NP_001269525.1:n.512-134_512-133del
NM_021181.4:c.937-134_937-133del	NP_067004.3:n.937-134_937-133del
ENST00000359331.8:c.833-134_833-133del	ENSP00000352281.4:n.833-134_833-133del
ENST00000368042.7:c.616-134_616-133del	ENSP00000357021.3:n.616-134_616-133del
ENST00000368043.7:c.937-134_937-133del	ENSP00000357022.3:n.937-134_937-133del
ENST00000441662.6:c.544-134_544-133del	ENSP00000405605.2:n.544-134_544-133del
ENST00000444090.6:c.440-134_440-133del	ENSP00000416592.2:n.440-134_440-133del
ENST00000458104.6:c.392-134_392-133del	ENSP00000403294.2:n.392-134_392-133del
ENST00000458602.6:c.496-134_496-133del	ENSP00000409965.2:n.496-134_496-133del
ENST00000484221.1:n.1827-134_1827-133del
ENST00000621377.4:c.655-134_655-133del	ENSP00000483774.1:n.655-134_655-133del
XM_005245386.1:c.817-134_817-133del	XP_005245443.1:n.817-134_817-133del
XM_006711471.1:c.713-134_713-133del	XP_006711534.1:n.713-134_713-133del
XM_011509828.1:c.976-134_976-133del	XP_011508130.1:n.976-134_976-133del
XM_011509829.1:c.872-134_872-133del	XP_011508131.1:n.872-134_872-133del
XM_024448757.1:c.1147-134_1147-133del	XP_024304525.1:n.1147-134_1147-133del