Canonical Allele Identifier: CA2275147046

Gene: CD300LF RAB37

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74695842C= , CM000679.2:g.74695842C=	GRCh38
NC_000017.10:g.72691981C= , CM000679.1:g.72691981C=	GRCh37
NC_000017.9:g.70203576C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326165.11:c.600G= (CD300LF) MANE Select	ENSP00000327075.6:p.Glu200=
ENST00000301573.13:c.646G= (CD300LF)	ENSP00000301573.9:p.Gly216=
ENST00000326165.10:c.600G= (CD300LF)	ENSP00000327075.6:p.Glu200=
ENST00000340415.7:c.72+24184C= (RAB37)	ENSP00000341354.3:n.72+24184C=
ENST00000343125.8:c.496G= (CD300LF)	ENSP00000343751.4:p.Gly166=
ENST00000361254.8:c.631G= (CD300LF)	ENSP00000355294.4:p.Gly211=
ENST00000392617.7:n.479+24184C= (RAB37)
ENST00000402449.8:c.72+24184C= (RAB37)	ENSP00000383934.4:n.72+24184C=
ENST00000462044.5:c.473G= (CD300LF)	ENSP00000464223.1:p.Arg158=
ENST00000464910.5:c.609G= (CD300LF)	ENSP00000464257.1:p.Glu203=
ENST00000469092.5:c.496G= (CD300LF)	ENSP00000463743.1:p.Gly166=
ENST00000581500.1:c.631G= (CD300LF)	ENSP00000464610.1:p.Gly211=
ENST00000583937.5:c.645G= (CD300LF)	ENSP00000462309.1:p.Glu215=
NM_001289082.1:c.496G= (CD300LF)	NP_001276011.1:p.Gly166=
NM_001289083.1:c.646G= (CD300LF)	NP_001276012.1:p.Gly216=
NM_001289084.1:c.645G= (CD300LF)	NP_001276013.1:p.Glu215=
NM_001289085.1:c.609G= (CD300LF)	NP_001276014.1:p.Glu203=
NM_001289086.1:c.631G= (CD300LF)	NP_001276015.1:p.Gly211=
NM_001289087.1:c.577G= (CD300LF)	NP_001276016.1:p.Gly193=
NM_139018.4:c.600G= (CD300LF)	NP_620587.2:p.Glu200=
NM_175738.4:c.72+24184C= (RAB37)	NP_783865.1:n.72+24184C=
NR_110298.1:n.772G= (CD300LF)
XM_011524369.1:c.732G= (CD300LF)	XP_011522671.1:p.Glu244=
XM_011524370.1:c.723G= (CD300LF)	XP_011522672.1:p.Glu241=
XM_011524371.1:c.723G= (CD300LF)	XP_011522673.1:p.Glu241=
XM_011524372.1:c.687G= (CD300LF)	XP_011522674.1:p.Glu229=
XM_011524373.1:c.678G= (CD300LF)	XP_011522675.1:p.Glu226=
XM_011524374.1:c.678G= (CD300LF)	XP_011522676.1:p.Glu226=
XM_011524375.1:c.654G= (CD300LF)	XP_011522677.1:p.Glu218=
XM_011524376.1:c.709G= (CD300LF)	XP_011522678.1:p.Gly237=
XM_011524377.1:c.709G= (CD300LF)	XP_011522679.1:p.Gly237=
XM_011524378.1:c.700G= (CD300LF)	XP_011522680.1:p.Gly234=
XM_011524379.1:c.664G= (CD300LF)	XP_011522681.1:p.Gly222=
XM_017024212.2:c.657G= (CD300LF)	XP_016879701.1:p.Glu219=
XM_017024213.2:c.712G= (CD300LF)	XP_016879702.1:p.Gly238=
XM_017024214.2:c.703G= (CD300LF)	XP_016879703.1:p.Gly235=
XM_017024215.1:c.655G= (CD300LF)	XP_016879704.1:p.Gly219=
XM_017024216.2:c.634G= (CD300LF)	XP_016879705.1:p.Gly212=
XM_017024217.2:c.622G= (CD300LF)	XP_016879706.1:p.Gly208=
NM_139018.5:c.600G= (CD300LF) MANE Select	NP_620587.2:p.Glu200=
NM_001289082.2:c.496G= (CD300LF)	NP_001276011.1:p.Gly166=
NM_001289083.2:c.646G= (CD300LF)	NP_001276012.1:p.Gly216=
NM_001289084.2:c.645G= (CD300LF)	NP_001276013.1:p.Glu215=
NM_001289085.2:c.609G= (CD300LF)	NP_001276014.1:p.Glu203=
NM_001289086.2:c.631G= (CD300LF)	NP_001276015.1:p.Gly211=
NM_001289087.2:c.577G= (CD300LF)	NP_001276016.1:p.Gly193=
NM_175738.5:c.72+24184C= (RAB37)	NP_783865.1:n.72+24184C=
NR_110298.2:n.695G= (CD300LF)