Canonical Allele Identifier: CA2275147044

Gene: CD300LF RAB37

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74695839G= , CM000679.2:g.74695839G=	GRCh38
NC_000017.10:g.72691978G= , CM000679.1:g.72691978G=	GRCh37
NC_000017.9:g.70203573G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326165.11:c.603C= (CD300LF) MANE Select	ENSP00000327075.6:p.Gly201=
ENST00000301573.13:c.649C= (CD300LF)	ENSP00000301573.9:p.Arg217=
ENST00000326165.10:c.603C= (CD300LF)	ENSP00000327075.6:p.Gly201=
ENST00000340415.7:c.72+24181G= (RAB37)	ENSP00000341354.3:n.72+24181G=
ENST00000343125.8:c.499C= (CD300LF)	ENSP00000343751.4:p.Arg167=
ENST00000361254.8:c.634C= (CD300LF)	ENSP00000355294.4:p.Arg212=
ENST00000392617.7:n.479+24181G= (RAB37)
ENST00000402449.8:c.72+24181G= (RAB37)	ENSP00000383934.4:n.72+24181G=
ENST00000462044.5:c.476C= (CD300LF)	ENSP00000464223.1:p.Ala159=
ENST00000464910.5:c.612C= (CD300LF)	ENSP00000464257.1:p.Gly204=
ENST00000469092.5:c.499C= (CD300LF)	ENSP00000463743.1:p.Arg167=
ENST00000581500.1:c.634C= (CD300LF)	ENSP00000464610.1:p.Arg212=
ENST00000583937.5:c.648C= (CD300LF)	ENSP00000462309.1:p.Gly216=
NM_001289082.1:c.499C= (CD300LF)	NP_001276011.1:p.Arg167=
NM_001289083.1:c.649C= (CD300LF)	NP_001276012.1:p.Arg217=
NM_001289084.1:c.648C= (CD300LF)	NP_001276013.1:p.Gly216=
NM_001289085.1:c.612C= (CD300LF)	NP_001276014.1:p.Gly204=
NM_001289086.1:c.634C= (CD300LF)	NP_001276015.1:p.Arg212=
NM_001289087.1:c.580C= (CD300LF)	NP_001276016.1:p.Arg194=
NM_139018.4:c.603C= (CD300LF)	NP_620587.2:p.Gly201=
NM_175738.4:c.72+24181G= (RAB37)	NP_783865.1:n.72+24181G=
NR_110298.1:n.775C= (CD300LF)
XM_011524369.1:c.735C= (CD300LF)	XP_011522671.1:p.Gly245=
XM_011524370.1:c.726C= (CD300LF)	XP_011522672.1:p.Gly242=
XM_011524371.1:c.726C= (CD300LF)	XP_011522673.1:p.Gly242=
XM_011524372.1:c.690C= (CD300LF)	XP_011522674.1:p.Gly230=
XM_011524373.1:c.681C= (CD300LF)	XP_011522675.1:p.Gly227=
XM_011524374.1:c.681C= (CD300LF)	XP_011522676.1:p.Gly227=
XM_011524375.1:c.657C= (CD300LF)	XP_011522677.1:p.Gly219=
XM_011524376.1:c.712C= (CD300LF)	XP_011522678.1:p.Arg238=
XM_011524377.1:c.712C= (CD300LF)	XP_011522679.1:p.Arg238=
XM_011524378.1:c.703C= (CD300LF)	XP_011522680.1:p.Arg235=
XM_011524379.1:c.667C= (CD300LF)	XP_011522681.1:p.Arg223=
XM_017024212.2:c.660C= (CD300LF)	XP_016879701.1:p.Gly220=
XM_017024213.2:c.715C= (CD300LF)	XP_016879702.1:p.Arg239=
XM_017024214.2:c.706C= (CD300LF)	XP_016879703.1:p.Arg236=
XM_017024215.1:c.658C= (CD300LF)	XP_016879704.1:p.Arg220=
XM_017024216.2:c.637C= (CD300LF)	XP_016879705.1:p.Arg213=
XM_017024217.2:c.625C= (CD300LF)	XP_016879706.1:p.Arg209=
NM_139018.5:c.603C= (CD300LF) MANE Select	NP_620587.2:p.Gly201=
NM_001289082.2:c.499C= (CD300LF)	NP_001276011.1:p.Arg167=
NM_001289083.2:c.649C= (CD300LF)	NP_001276012.1:p.Arg217=
NM_001289084.2:c.648C= (CD300LF)	NP_001276013.1:p.Gly216=
NM_001289085.2:c.612C= (CD300LF)	NP_001276014.1:p.Gly204=
NM_001289086.2:c.634C= (CD300LF)	NP_001276015.1:p.Arg212=
NM_001289087.2:c.580C= (CD300LF)	NP_001276016.1:p.Arg194=
NM_175738.5:c.72+24181G= (RAB37)	NP_783865.1:n.72+24181G=
NR_110298.2:n.698C= (CD300LF)