Canonical Allele Identifier: CA400935184

Gene: CD300LF RAB37

Linked Data

• MyVariant Identifiers: chr17:g.72691974G>C (hg19) ; chr17:g.74695835G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74695835G>C , CM000679.2:g.74695835G>C	GRCh38
NC_000017.10:g.72691974G>C , CM000679.1:g.72691974G>C	GRCh37
NC_000017.9:g.70203569G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326165.11:c.607C>G (CD300LF) MANE Select	ENSP00000327075.6:p.Leu203Val
ENST00000301573.13:c.653C>G (CD300LF)	ENSP00000301573.9:p.Pro218Arg
ENST00000326165.10:c.607C>G (CD300LF)	ENSP00000327075.6:p.Leu203Val
ENST00000340415.7:c.72+24177G>C (RAB37)	ENSP00000341354.3:n.72+24177G>C
ENST00000343125.8:c.503C>G (CD300LF)	ENSP00000343751.4:p.Pro168Arg
ENST00000361254.8:c.638C>G (CD300LF)	ENSP00000355294.4:p.Pro213Arg
ENST00000392617.7:n.479+24177G>C (RAB37)
ENST00000402449.8:c.72+24177G>C (RAB37)	ENSP00000383934.4:n.72+24177G>C
ENST00000462044.5:c.480C>G (CD300LF)	ENSP00000464223.1:p.Thr160=
ENST00000464910.5:c.616C>G (CD300LF)	ENSP00000464257.1:p.Leu206Val
ENST00000469092.5:c.503C>G (CD300LF)	ENSP00000463743.1:p.Pro168Arg
ENST00000581500.1:c.638C>G (CD300LF)	ENSP00000464610.1:p.Pro213Arg
ENST00000583937.5:c.652C>G (CD300LF)	ENSP00000462309.1:p.Leu218Val
NM_001289082.1:c.503C>G (CD300LF)	NP_001276011.1:p.Pro168Arg
NM_001289083.1:c.653C>G (CD300LF)	NP_001276012.1:p.Pro218Arg
NM_001289084.1:c.652C>G (CD300LF)	NP_001276013.1:p.Leu218Val
NM_001289085.1:c.616C>G (CD300LF)	NP_001276014.1:p.Leu206Val
NM_001289086.1:c.638C>G (CD300LF)	NP_001276015.1:p.Pro213Arg
NM_001289087.1:c.584C>G (CD300LF)	NP_001276016.1:p.Pro195Arg
NM_139018.4:c.607C>G (CD300LF)	NP_620587.2:p.Leu203Val
NM_175738.4:c.72+24177G>C (RAB37)	NP_783865.1:n.72+24177G>C
NR_110298.1:n.779C>G (CD300LF)
XM_011524369.1:c.739C>G (CD300LF)	XP_011522671.1:p.Leu247Val
XM_011524370.1:c.730C>G (CD300LF)	XP_011522672.1:p.Leu244Val
XM_011524371.1:c.730C>G (CD300LF)	XP_011522673.1:p.Leu244Val
XM_011524372.1:c.694C>G (CD300LF)	XP_011522674.1:p.Leu232Val
XM_011524373.1:c.685C>G (CD300LF)	XP_011522675.1:p.Leu229Val
XM_011524374.1:c.685C>G (CD300LF)	XP_011522676.1:p.Leu229Val
XM_011524375.1:c.661C>G (CD300LF)	XP_011522677.1:p.Leu221Val
XM_011524376.1:c.716C>G (CD300LF)	XP_011522678.1:p.Pro239Arg
XM_011524377.1:c.716C>G (CD300LF)	XP_011522679.1:p.Pro239Arg
XM_011524378.1:c.707C>G (CD300LF)	XP_011522680.1:p.Pro236Arg
XM_011524379.1:c.671C>G (CD300LF)	XP_011522681.1:p.Pro224Arg
XM_017024212.2:c.664C>G (CD300LF)	XP_016879701.1:p.Leu222Val
XM_017024213.2:c.719C>G (CD300LF)	XP_016879702.1:p.Pro240Arg
XM_017024214.2:c.710C>G (CD300LF)	XP_016879703.1:p.Pro237Arg
XM_017024215.1:c.662C>G (CD300LF)	XP_016879704.1:p.Pro221Arg
XM_017024216.2:c.641C>G (CD300LF)	XP_016879705.1:p.Pro214Arg
XM_017024217.2:c.629C>G (CD300LF)	XP_016879706.1:p.Pro210Arg
NM_139018.5:c.607C>G (CD300LF) MANE Select	NP_620587.2:p.Leu203Val
NM_001289082.2:c.503C>G (CD300LF)	NP_001276011.1:p.Pro168Arg
NM_001289083.2:c.653C>G (CD300LF)	NP_001276012.1:p.Pro218Arg
NM_001289084.2:c.652C>G (CD300LF)	NP_001276013.1:p.Leu218Val
NM_001289085.2:c.616C>G (CD300LF)	NP_001276014.1:p.Leu206Val
NM_001289086.2:c.638C>G (CD300LF)	NP_001276015.1:p.Pro213Arg
NM_001289087.2:c.584C>G (CD300LF)	NP_001276016.1:p.Pro195Arg
NM_175738.5:c.72+24177G>C (RAB37)	NP_783865.1:n.72+24177G>C
NR_110298.2:n.702C>G (CD300LF)