Canonical Allele Identifier: CA2275146995

Gene: CD300LF RAB37

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74695758C= , CM000679.2:g.74695758C=	GRCh38
NC_000017.10:g.72691897C= , CM000679.1:g.72691897C=	GRCh37
NC_000017.9:g.70203492C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326165.11:c.684G= (CD300LF) MANE Select	ENSP00000327075.6:p.Gln228=
ENST00000301573.13:c.730G= (CD300LF)	ENSP00000301573.9:p.Gly244=
ENST00000326165.10:c.684G= (CD300LF)	ENSP00000327075.6:p.Gln228=
ENST00000340415.7:c.72+24100C= (RAB37)	ENSP00000341354.3:n.72+24100C=
ENST00000343125.8:c.580G= (CD300LF)	ENSP00000343751.4:p.Gly194=
ENST00000361254.8:c.715G= (CD300LF)	ENSP00000355294.4:p.Gly239=
ENST00000392617.7:n.479+24100C= (RAB37)
ENST00000402449.8:c.72+24100C= (RAB37)	ENSP00000383934.4:n.72+24100C=
ENST00000462044.5:c.*59G= (CD300LF)	ENSP00000464223.1:n.*59G=
ENST00000464910.5:c.693G= (CD300LF)	ENSP00000464257.1:p.Gln231=
ENST00000469092.5:c.580G= (CD300LF)	ENSP00000463743.1:p.Gly194=
ENST00000581500.1:c.715G= (CD300LF)	ENSP00000464610.1:p.Gly239=
ENST00000583937.5:c.729G= (CD300LF)	ENSP00000462309.1:p.Gln243=
NM_001289082.1:c.580G= (CD300LF)	NP_001276011.1:p.Gly194=
NM_001289083.1:c.730G= (CD300LF)	NP_001276012.1:p.Gly244=
NM_001289084.1:c.729G= (CD300LF)	NP_001276013.1:p.Gln243=
NM_001289085.1:c.693G= (CD300LF)	NP_001276014.1:p.Gln231=
NM_001289086.1:c.715G= (CD300LF)	NP_001276015.1:p.Gly239=
NM_001289087.1:c.661G= (CD300LF)	NP_001276016.1:p.Gly221=
NM_139018.4:c.684G= (CD300LF)	NP_620587.2:p.Gln228=
NM_175738.4:c.72+24100C= (RAB37)	NP_783865.1:n.72+24100C=
NR_110298.1:n.856G= (CD300LF)
XM_011524369.1:c.816G= (CD300LF)	XP_011522671.1:p.Gln272=
XM_011524370.1:c.807G= (CD300LF)	XP_011522672.1:p.Gln269=
XM_011524371.1:c.807G= (CD300LF)	XP_011522673.1:p.Gln269=
XM_011524372.1:c.771G= (CD300LF)	XP_011522674.1:p.Gln257=
XM_011524373.1:c.762G= (CD300LF)	XP_011522675.1:p.Gln254=
XM_011524374.1:c.762G= (CD300LF)	XP_011522676.1:p.Gln254=
XM_011524375.1:c.738G= (CD300LF)	XP_011522677.1:p.Gln246=
XM_011524376.1:c.793G= (CD300LF)	XP_011522678.1:p.Gly265=
XM_011524377.1:c.793G= (CD300LF)	XP_011522679.1:p.Gly265=
XM_011524378.1:c.784G= (CD300LF)	XP_011522680.1:p.Gly262=
XM_011524379.1:c.748G= (CD300LF)	XP_011522681.1:p.Gly250=
XM_017024212.2:c.741G= (CD300LF)	XP_016879701.1:p.Gln247=
XM_017024213.2:c.796G= (CD300LF)	XP_016879702.1:p.Gly266=
XM_017024214.2:c.787G= (CD300LF)	XP_016879703.1:p.Gly263=
XM_017024215.1:c.739G= (CD300LF)	XP_016879704.1:p.Gly247=
XM_017024216.2:c.718G= (CD300LF)	XP_016879705.1:p.Gly240=
XM_017024217.2:c.706G= (CD300LF)	XP_016879706.1:p.Gly236=
NM_139018.5:c.684G= (CD300LF) MANE Select	NP_620587.2:p.Gln228=
NM_001289082.2:c.580G= (CD300LF)	NP_001276011.1:p.Gly194=
NM_001289083.2:c.730G= (CD300LF)	NP_001276012.1:p.Gly244=
NM_001289084.2:c.729G= (CD300LF)	NP_001276013.1:p.Gln243=
NM_001289085.2:c.693G= (CD300LF)	NP_001276014.1:p.Gln231=
NM_001289086.2:c.715G= (CD300LF)	NP_001276015.1:p.Gly239=
NM_001289087.2:c.661G= (CD300LF)	NP_001276016.1:p.Gly221=
NM_175738.5:c.72+24100C= (RAB37)	NP_783865.1:n.72+24100C=
NR_110298.2:n.779G= (CD300LF)