Canonical Allele Identifier: CA400934971

Gene: CD300LF RAB37

Linked Data

• dbSNP Id: rs774062854
• MyVariant Identifiers: chr17:g.72691895A>C (hg19) ; chr17:g.74695756A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74695756A>C , CM000679.2:g.74695756A>C	GRCh38
NC_000017.10:g.72691895A>C , CM000679.1:g.72691895A>C	GRCh37
NC_000017.9:g.70203490A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326165.11:c.686T>G (CD300LF) MANE Select	ENSP00000327075.6:p.Val229Gly
ENST00000301573.13:c.732T>G (CD300LF)	ENSP00000301573.9:p.Gly244=
ENST00000326165.10:c.686T>G (CD300LF)	ENSP00000327075.6:p.Val229Gly
ENST00000340415.7:c.72+24098A>C (RAB37)	ENSP00000341354.3:n.72+24098A>C
ENST00000343125.8:c.582T>G (CD300LF)	ENSP00000343751.4:p.Gly194=
ENST00000361254.8:c.717T>G (CD300LF)	ENSP00000355294.4:p.Gly239=
ENST00000392617.7:n.479+24098A>C (RAB37)
ENST00000402449.8:c.72+24098A>C (RAB37)	ENSP00000383934.4:n.72+24098A>C
ENST00000462044.5:c.*61T>G (CD300LF)	ENSP00000464223.1:n.*61T>G
ENST00000464910.5:c.695T>G (CD300LF)	ENSP00000464257.1:p.Val232Gly
ENST00000469092.5:c.582T>G (CD300LF)	ENSP00000463743.1:p.Gly194=
ENST00000581500.1:c.717T>G (CD300LF)	ENSP00000464610.1:p.Gly239=
ENST00000583937.5:c.731T>G (CD300LF)	ENSP00000462309.1:p.Val244Gly
NM_001289082.1:c.582T>G (CD300LF)	NP_001276011.1:p.Gly194=
NM_001289083.1:c.732T>G (CD300LF)	NP_001276012.1:p.Gly244=
NM_001289084.1:c.731T>G (CD300LF)	NP_001276013.1:p.Val244Gly
NM_001289085.1:c.695T>G (CD300LF)	NP_001276014.1:p.Val232Gly
NM_001289086.1:c.717T>G (CD300LF)	NP_001276015.1:p.Gly239=
NM_001289087.1:c.663T>G (CD300LF)	NP_001276016.1:p.Gly221=
NM_139018.4:c.686T>G (CD300LF)	NP_620587.2:p.Val229Gly
NM_175738.4:c.72+24098A>C (RAB37)	NP_783865.1:n.72+24098A>C
NR_110298.1:n.858T>G (CD300LF)
XM_011524369.1:c.818T>G (CD300LF)	XP_011522671.1:p.Val273Gly
XM_011524370.1:c.809T>G (CD300LF)	XP_011522672.1:p.Val270Gly
XM_011524371.1:c.809T>G (CD300LF)	XP_011522673.1:p.Val270Gly
XM_011524372.1:c.773T>G (CD300LF)	XP_011522674.1:p.Val258Gly
XM_011524373.1:c.764T>G (CD300LF)	XP_011522675.1:p.Val255Gly
XM_011524374.1:c.764T>G (CD300LF)	XP_011522676.1:p.Val255Gly
XM_011524375.1:c.740T>G (CD300LF)	XP_011522677.1:p.Val247Gly
XM_011524376.1:c.795T>G (CD300LF)	XP_011522678.1:p.Gly265=
XM_011524377.1:c.795T>G (CD300LF)	XP_011522679.1:p.Gly265=
XM_011524378.1:c.786T>G (CD300LF)	XP_011522680.1:p.Gly262=
XM_011524379.1:c.750T>G (CD300LF)	XP_011522681.1:p.Gly250=
XM_017024212.2:c.743T>G (CD300LF)	XP_016879701.1:p.Val248Gly
XM_017024213.2:c.798T>G (CD300LF)	XP_016879702.1:p.Gly266=
XM_017024214.2:c.789T>G (CD300LF)	XP_016879703.1:p.Gly263=
XM_017024215.1:c.741T>G (CD300LF)	XP_016879704.1:p.Gly247=
XM_017024216.2:c.720T>G (CD300LF)	XP_016879705.1:p.Gly240=
XM_017024217.2:c.708T>G (CD300LF)	XP_016879706.1:p.Gly236=
NM_139018.5:c.686T>G (CD300LF) MANE Select	NP_620587.2:p.Val229Gly
NM_001289082.2:c.582T>G (CD300LF)	NP_001276011.1:p.Gly194=
NM_001289083.2:c.732T>G (CD300LF)	NP_001276012.1:p.Gly244=
NM_001289084.2:c.731T>G (CD300LF)	NP_001276013.1:p.Val244Gly
NM_001289085.2:c.695T>G (CD300LF)	NP_001276014.1:p.Val232Gly
NM_001289086.2:c.717T>G (CD300LF)	NP_001276015.1:p.Gly239=
NM_001289087.2:c.663T>G (CD300LF)	NP_001276016.1:p.Gly221=
NM_175738.5:c.72+24098A>C (RAB37)	NP_783865.1:n.72+24098A>C
NR_110298.2:n.781T>G (CD300LF)