Canonical Allele Identifier: CA400935035

Gene: CD300LF RAB37

Linked Data

• dbSNP Id: rs2032398822
• gnomAD v3: 17-74695779-G-A
• gnomAD v4: 17-74695779-G-A
• MyVariant Identifiers: chr17:g.72691918G>A (hg19) ; chr17:g.74695779G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74695779G>A , CM000679.2:g.74695779G>A	GRCh38
NC_000017.10:g.72691918G>A , CM000679.1:g.72691918G>A	GRCh37
NC_000017.9:g.70203513G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326165.11:c.663C>T (CD300LF) MANE Select	ENSP00000327075.6:p.Thr221=
ENST00000301573.13:c.709C>T (CD300LF)	ENSP00000301573.9:p.His237Tyr
ENST00000326165.10:c.663C>T (CD300LF)	ENSP00000327075.6:p.Thr221=
ENST00000340415.7:c.72+24121G>A (RAB37)	ENSP00000341354.3:n.72+24121G>A
ENST00000343125.8:c.559C>T (CD300LF)	ENSP00000343751.4:p.His187Tyr
ENST00000361254.8:c.694C>T (CD300LF)	ENSP00000355294.4:p.His232Tyr
ENST00000392617.7:n.479+24121G>A (RAB37)
ENST00000402449.8:c.72+24121G>A (RAB37)	ENSP00000383934.4:n.72+24121G>A
ENST00000462044.5:c.*38C>T (CD300LF)	ENSP00000464223.1:n.*38C>T
ENST00000464910.5:c.672C>T (CD300LF)	ENSP00000464257.1:p.Thr224=
ENST00000469092.5:c.559C>T (CD300LF)	ENSP00000463743.1:p.His187Tyr
ENST00000581500.1:c.694C>T (CD300LF)	ENSP00000464610.1:p.His232Tyr
ENST00000583937.5:c.708C>T (CD300LF)	ENSP00000462309.1:p.Thr236=
NM_001289082.1:c.559C>T (CD300LF)	NP_001276011.1:p.His187Tyr
NM_001289083.1:c.709C>T (CD300LF)	NP_001276012.1:p.His237Tyr
NM_001289084.1:c.708C>T (CD300LF)	NP_001276013.1:p.Thr236=
NM_001289085.1:c.672C>T (CD300LF)	NP_001276014.1:p.Thr224=
NM_001289086.1:c.694C>T (CD300LF)	NP_001276015.1:p.His232Tyr
NM_001289087.1:c.640C>T (CD300LF)	NP_001276016.1:p.His214Tyr
NM_139018.4:c.663C>T (CD300LF)	NP_620587.2:p.Thr221=
NM_175738.4:c.72+24121G>A (RAB37)	NP_783865.1:n.72+24121G>A
NR_110298.1:n.835C>T (CD300LF)
XM_011524369.1:c.795C>T (CD300LF)	XP_011522671.1:p.Thr265=
XM_011524370.1:c.786C>T (CD300LF)	XP_011522672.1:p.Thr262=
XM_011524371.1:c.786C>T (CD300LF)	XP_011522673.1:p.Thr262=
XM_011524372.1:c.750C>T (CD300LF)	XP_011522674.1:p.Thr250=
XM_011524373.1:c.741C>T (CD300LF)	XP_011522675.1:p.Thr247=
XM_011524374.1:c.741C>T (CD300LF)	XP_011522676.1:p.Thr247=
XM_011524375.1:c.717C>T (CD300LF)	XP_011522677.1:p.Thr239=
XM_011524376.1:c.772C>T (CD300LF)	XP_011522678.1:p.His258Tyr
XM_011524377.1:c.772C>T (CD300LF)	XP_011522679.1:p.His258Tyr
XM_011524378.1:c.763C>T (CD300LF)	XP_011522680.1:p.His255Tyr
XM_011524379.1:c.727C>T (CD300LF)	XP_011522681.1:p.His243Tyr
XM_017024212.2:c.720C>T (CD300LF)	XP_016879701.1:p.Thr240=
XM_017024213.2:c.775C>T (CD300LF)	XP_016879702.1:p.His259Tyr
XM_017024214.2:c.766C>T (CD300LF)	XP_016879703.1:p.His256Tyr
XM_017024215.1:c.718C>T (CD300LF)	XP_016879704.1:p.His240Tyr
XM_017024216.2:c.697C>T (CD300LF)	XP_016879705.1:p.His233Tyr
XM_017024217.2:c.685C>T (CD300LF)	XP_016879706.1:p.His229Tyr
NM_139018.5:c.663C>T (CD300LF) MANE Select	NP_620587.2:p.Thr221=
NM_001289082.2:c.559C>T (CD300LF)	NP_001276011.1:p.His187Tyr
NM_001289083.2:c.709C>T (CD300LF)	NP_001276012.1:p.His237Tyr
NM_001289084.2:c.708C>T (CD300LF)	NP_001276013.1:p.Thr236=
NM_001289085.2:c.672C>T (CD300LF)	NP_001276014.1:p.Thr224=
NM_001289086.2:c.694C>T (CD300LF)	NP_001276015.1:p.His232Tyr
NM_001289087.2:c.640C>T (CD300LF)	NP_001276016.1:p.His214Tyr
NM_175738.5:c.72+24121G>A (RAB37)	NP_783865.1:n.72+24121G>A
NR_110298.2:n.758C>T (CD300LF)