Canonical Allele Identifier: CA2275147133

Gene: CD300LF RAB37

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74696039C= , CM000679.2:g.74696039C=	GRCh38
NC_000017.10:g.72692178C= , CM000679.1:g.72692178C=	GRCh37
NC_000017.9:g.70203773C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326165.11:c.582+156G= (CD300LF) MANE Select	ENSP00000327075.6:n.582+156G=
ENST00000301573.13:c.628+156G= (CD300LF)	ENSP00000301573.9:n.628+156G=
ENST00000326165.10:c.582+156G= (CD300LF)	ENSP00000327075.6:n.582+156G=
ENST00000340415.7:c.72+24381C= (RAB37)	ENSP00000341354.3:n.72+24381C=
ENST00000343125.8:c.478+156G= (CD300LF)	ENSP00000343751.4:n.478+156G=
ENST00000361254.8:c.614-180G= (CD300LF)	ENSP00000355294.4:n.614-180G=
ENST00000392617.7:n.479+24381C= (RAB37)
ENST00000402449.8:c.72+24381C= (RAB37)	ENSP00000383934.4:n.72+24381C=
ENST00000462044.5:c.456-180G= (CD300LF)	ENSP00000464223.1:n.456-180G=
ENST00000464910.5:c.591+156G= (CD300LF)	ENSP00000464257.1:n.591+156G=
ENST00000469092.5:c.478+156G= (CD300LF)	ENSP00000463743.1:n.478+156G=
ENST00000581500.1:c.614-180G= (CD300LF)	ENSP00000464610.1:n.614-180G=
ENST00000583937.5:c.627+156G= (CD300LF)	ENSP00000462309.1:n.627+156G=
NM_001289082.1:c.478+156G= (CD300LF)	NP_001276011.1:n.478+156G=
NM_001289083.1:c.628+156G= (CD300LF)	NP_001276012.1:n.628+156G=
NM_001289084.1:c.627+156G= (CD300LF)	NP_001276013.1:n.627+156G=
NM_001289085.1:c.591+156G= (CD300LF)	NP_001276014.1:n.591+156G=
NM_001289086.1:c.614-180G= (CD300LF)	NP_001276015.1:n.614-180G=
NM_001289087.1:c.560-180G= (CD300LF)	NP_001276016.1:n.560-180G=
NM_139018.4:c.582+156G= (CD300LF)	NP_620587.2:n.582+156G=
NM_175738.4:c.72+24381C= (RAB37)	NP_783865.1:n.72+24381C=
NR_110298.1:n.755-180G= (CD300LF)
XM_011524369.1:c.714+156G= (CD300LF)	XP_011522671.1:n.714+156G=
XM_011524370.1:c.705+156G= (CD300LF)	XP_011522672.1:n.705+156G=
XM_011524371.1:c.705+156G= (CD300LF)	XP_011522673.1:n.705+156G=
XM_011524372.1:c.669+156G= (CD300LF)	XP_011522674.1:n.669+156G=
XM_011524373.1:c.660+156G= (CD300LF)	XP_011522675.1:n.660+156G=
XM_011524374.1:c.660+156G= (CD300LF)	XP_011522676.1:n.660+156G=
XM_011524375.1:c.636+156G= (CD300LF)	XP_011522677.1:n.636+156G=
XM_011524376.1:c.691+156G= (CD300LF)	XP_011522678.1:n.691+156G=
XM_011524377.1:c.692-180G= (CD300LF)	XP_011522679.1:n.692-180G=
XM_011524378.1:c.682+156G= (CD300LF)	XP_011522680.1:n.682+156G=
XM_011524379.1:c.646+156G= (CD300LF)	XP_011522681.1:n.646+156G=
XM_017024212.2:c.639+156G= (CD300LF)	XP_016879701.1:n.639+156G=
XM_017024213.2:c.694+156G= (CD300LF)	XP_016879702.1:n.694+156G=
XM_017024214.2:c.685+156G= (CD300LF)	XP_016879703.1:n.685+156G=
XM_017024215.1:c.637+156G= (CD300LF)	XP_016879704.1:n.637+156G=
XM_017024216.2:c.617-180G= (CD300LF)	XP_016879705.1:n.617-180G=
XM_017024217.2:c.605-180G= (CD300LF)	XP_016879706.1:n.605-180G=
NM_139018.5:c.582+156G= (CD300LF) MANE Select	NP_620587.2:n.582+156G=
NM_001289082.2:c.478+156G= (CD300LF)	NP_001276011.1:n.478+156G=
NM_001289083.2:c.628+156G= (CD300LF)	NP_001276012.1:n.628+156G=
NM_001289084.2:c.627+156G= (CD300LF)	NP_001276013.1:n.627+156G=
NM_001289085.2:c.591+156G= (CD300LF)	NP_001276014.1:n.591+156G=
NM_001289086.2:c.614-180G= (CD300LF)	NP_001276015.1:n.614-180G=
NM_001289087.2:c.560-180G= (CD300LF)	NP_001276016.1:n.560-180G=
NM_175738.5:c.72+24381C= (RAB37)	NP_783865.1:n.72+24381C=
NR_110298.2:n.678-180G= (CD300LF)