Canonical Allele Identifier: CA400935241

Gene: CD300LF RAB37

Linked Data

• dbSNP Id: rs2143550296
• MyVariant Identifiers: chr17:g.72691996T>C (hg19) ; chr17:g.74695857T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74695857T>C , CM000679.2:g.74695857T>C	GRCh38
NC_000017.10:g.72691996T>C , CM000679.1:g.72691996T>C	GRCh37
NC_000017.9:g.70203591T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326165.11:c.585A>G (CD300LF) MANE Select	ENSP00000327075.6:p.Val195=
ENST00000301573.13:c.631A>G (CD300LF)	ENSP00000301573.9:p.Thr211Ala
ENST00000326165.10:c.585A>G (CD300LF)	ENSP00000327075.6:p.Val195=
ENST00000340415.7:c.72+24199T>C (RAB37)	ENSP00000341354.3:n.72+24199T>C
ENST00000343125.8:c.481A>G (CD300LF)	ENSP00000343751.4:p.Thr161Ala
ENST00000361254.8:c.616A>G (CD300LF)	ENSP00000355294.4:p.Thr206Ala
ENST00000392617.7:n.479+24199T>C (RAB37)
ENST00000402449.8:c.72+24199T>C (RAB37)	ENSP00000383934.4:n.72+24199T>C
ENST00000462044.5:c.458A>G (CD300LF)	ENSP00000464223.1:p.Tyr153Cys
ENST00000464910.5:c.594A>G (CD300LF)	ENSP00000464257.1:p.Val198=
ENST00000469092.5:c.481A>G (CD300LF)	ENSP00000463743.1:p.Thr161Ala
ENST00000581500.1:c.616A>G (CD300LF)	ENSP00000464610.1:p.Thr206Ala
ENST00000583937.5:c.630A>G (CD300LF)	ENSP00000462309.1:p.Val210=
NM_001289082.1:c.481A>G (CD300LF)	NP_001276011.1:p.Thr161Ala
NM_001289083.1:c.631A>G (CD300LF)	NP_001276012.1:p.Thr211Ala
NM_001289084.1:c.630A>G (CD300LF)	NP_001276013.1:p.Val210=
NM_001289085.1:c.594A>G (CD300LF)	NP_001276014.1:p.Val198=
NM_001289086.1:c.616A>G (CD300LF)	NP_001276015.1:p.Thr206Ala
NM_001289087.1:c.562A>G (CD300LF)	NP_001276016.1:p.Thr188Ala
NM_139018.4:c.585A>G (CD300LF)	NP_620587.2:p.Val195=
NM_175738.4:c.72+24199T>C (RAB37)	NP_783865.1:n.72+24199T>C
NR_110298.1:n.757A>G (CD300LF)
XM_011524369.1:c.717A>G (CD300LF)	XP_011522671.1:p.Val239=
XM_011524370.1:c.708A>G (CD300LF)	XP_011522672.1:p.Val236=
XM_011524371.1:c.708A>G (CD300LF)	XP_011522673.1:p.Val236=
XM_011524372.1:c.672A>G (CD300LF)	XP_011522674.1:p.Val224=
XM_011524373.1:c.663A>G (CD300LF)	XP_011522675.1:p.Val221=
XM_011524374.1:c.663A>G (CD300LF)	XP_011522676.1:p.Val221=
XM_011524375.1:c.639A>G (CD300LF)	XP_011522677.1:p.Val213=
XM_011524376.1:c.694A>G (CD300LF)	XP_011522678.1:p.Thr232Ala
XM_011524377.1:c.694A>G (CD300LF)	XP_011522679.1:p.Thr232Ala
XM_011524378.1:c.685A>G (CD300LF)	XP_011522680.1:p.Thr229Ala
XM_011524379.1:c.649A>G (CD300LF)	XP_011522681.1:p.Thr217Ala
XM_017024212.2:c.642A>G (CD300LF)	XP_016879701.1:p.Val214=
XM_017024213.2:c.697A>G (CD300LF)	XP_016879702.1:p.Thr233Ala
XM_017024214.2:c.688A>G (CD300LF)	XP_016879703.1:p.Thr230Ala
XM_017024215.1:c.640A>G (CD300LF)	XP_016879704.1:p.Thr214Ala
XM_017024216.2:c.619A>G (CD300LF)	XP_016879705.1:p.Thr207Ala
XM_017024217.2:c.607A>G (CD300LF)	XP_016879706.1:p.Thr203Ala
NM_139018.5:c.585A>G (CD300LF) MANE Select	NP_620587.2:p.Val195=
NM_001289082.2:c.481A>G (CD300LF)	NP_001276011.1:p.Thr161Ala
NM_001289083.2:c.631A>G (CD300LF)	NP_001276012.1:p.Thr211Ala
NM_001289084.2:c.630A>G (CD300LF)	NP_001276013.1:p.Val210=
NM_001289085.2:c.594A>G (CD300LF)	NP_001276014.1:p.Val198=
NM_001289086.2:c.616A>G (CD300LF)	NP_001276015.1:p.Thr206Ala
NM_001289087.2:c.562A>G (CD300LF)	NP_001276016.1:p.Thr188Ala
NM_175738.5:c.72+24199T>C (RAB37)	NP_783865.1:n.72+24199T>C
NR_110298.2:n.680A>G (CD300LF)