Canonical Allele Identifier: CA2648704016

Gene: SLAMF7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160752991G>T , CM000663.2:g.160752991G>T	GRCh38
NC_000001.10:g.160722781G>T , CM000663.1:g.160722781G>T	GRCh37
NC_000001.9:g.158989405G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021181.5:c.937-115G>T MANE Select	NP_067004.3:n.937-115G>T
ENST00000368043.8:c.937-115G>T MANE Select	ENSP00000357022.3:n.937-115G>T
NM_001282588.1:c.440-115G>T	NP_001269517.1:n.440-115G>T
NM_001282588.2:c.440-115G>T	NP_001269517.1:n.440-115G>T
NM_001282589.1:c.544-115G>T	NP_001269518.1:n.544-115G>T
NM_001282589.2:c.544-115G>T	NP_001269518.1:n.544-115G>T
NM_001282590.1:c.616-115G>T	NP_001269519.1:n.616-115G>T
NM_001282590.2:c.616-115G>T	NP_001269519.1:n.616-115G>T
NM_001282591.1:c.496-115G>T	NP_001269520.1:n.496-115G>T
NM_001282591.2:c.496-115G>T	NP_001269520.1:n.496-115G>T
NM_001282592.1:c.833-115G>T	NP_001269521.1:n.833-115G>T
NM_001282592.2:c.833-115G>T	NP_001269521.1:n.833-115G>T
NM_001282593.1:c.392-115G>T	NP_001269522.1:n.392-115G>T
NM_001282593.2:c.392-115G>T	NP_001269522.1:n.392-115G>T
NM_001282594.1:c.655-115G>T	NP_001269523.1:n.655-115G>T
NM_001282594.2:c.655-115G>T	NP_001269523.1:n.655-115G>T
NM_001282595.1:c.535-115G>T	NP_001269524.1:n.535-115G>T
NM_001282596.1:c.512-115G>T	NP_001269525.1:n.512-115G>T
NM_001282596.2:c.512-115G>T	NP_001269525.1:n.512-115G>T
NM_021181.4:c.937-115G>T	NP_067004.3:n.937-115G>T
ENST00000359331.8:c.833-115G>T	ENSP00000352281.4:n.833-115G>T
ENST00000368042.7:c.616-115G>T	ENSP00000357021.3:n.616-115G>T
ENST00000368043.7:c.937-115G>T	ENSP00000357022.3:n.937-115G>T
ENST00000441662.6:c.544-115G>T	ENSP00000405605.2:n.544-115G>T
ENST00000444090.6:c.440-115G>T	ENSP00000416592.2:n.440-115G>T
ENST00000458104.6:c.392-115G>T	ENSP00000403294.2:n.392-115G>T
ENST00000458602.6:c.496-115G>T	ENSP00000409965.2:n.496-115G>T
ENST00000484221.1:n.1827-115G>T
ENST00000621377.4:c.655-115G>T	ENSP00000483774.1:n.655-115G>T
XM_005245386.1:c.817-115G>T	XP_005245443.1:n.817-115G>T
XM_006711471.1:c.713-115G>T	XP_006711534.1:n.713-115G>T
XM_011509828.1:c.976-115G>T	XP_011508130.1:n.976-115G>T
XM_011509829.1:c.872-115G>T	XP_011508131.1:n.872-115G>T
XM_024448757.1:c.1147-115G>T	XP_024304525.1:n.1147-115G>T