Canonical Allele Identifier: CA400934891

Gene: CD300LF RAB37

Linked Data

• MyVariant Identifiers: chr17:g.72691871A>T (hg19) ; chr17:g.74695732A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74695732A>T , CM000679.2:g.74695732A>T	GRCh38
NC_000017.10:g.72691871A>T , CM000679.1:g.72691871A>T	GRCh37
NC_000017.9:g.70203466A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326165.11:c.710T>A (CD300LF) MANE Select	ENSP00000327075.6:p.Val237Asp
ENST00000301573.13:c.*21T>A (CD300LF)	ENSP00000301573.9:n.*21T>A
ENST00000326165.10:c.710T>A (CD300LF)	ENSP00000327075.6:p.Val237Asp
ENST00000340415.7:c.72+24074A>T (RAB37)	ENSP00000341354.3:n.72+24074A>T
ENST00000343125.8:c.606T>A (CD300LF)	ENSP00000343751.4:n.606T>A
ENST00000361254.8:c.741T>A (CD300LF)	ENSP00000355294.4:n.741T>A
ENST00000392617.7:n.479+24074A>T (RAB37)
ENST00000402449.8:c.72+24074A>T (RAB37)	ENSP00000383934.4:n.72+24074A>T
ENST00000462044.5:c.*85T>A (CD300LF)	ENSP00000464223.1:n.*85T>A
ENST00000464910.5:c.719T>A (CD300LF)	ENSP00000464257.1:p.Val240Asp
ENST00000469092.5:c.*21T>A (CD300LF)	ENSP00000463743.1:n.*21T>A
ENST00000583937.5:c.755T>A (CD300LF)	ENSP00000462309.1:p.Val252Asp
NM_001289082.1:c.*21T>A (CD300LF)	NP_001276011.1:n.*21T>A
NM_001289083.1:c.*21T>A (CD300LF)	NP_001276012.1:n.*21T>A
NM_001289084.1:c.755T>A (CD300LF)	NP_001276013.1:p.Val252Asp
NM_001289085.1:c.719T>A (CD300LF)	NP_001276014.1:p.Val240Asp
NM_001289086.1:c.*21T>A (CD300LF)	NP_001276015.1:n.*21T>A
NM_001289087.1:c.*21T>A (CD300LF)	NP_001276016.1:n.*21T>A
NM_139018.4:c.710T>A (CD300LF)	NP_620587.2:p.Val237Asp
NM_175738.4:c.72+24074A>T (RAB37)	NP_783865.1:n.72+24074A>T
NR_110298.1:n.882T>A (CD300LF)
XM_011524369.1:c.842T>A (CD300LF)	XP_011522671.1:p.Val281Asp
XM_011524370.1:c.833T>A (CD300LF)	XP_011522672.1:p.Val278Asp
XM_011524371.1:c.833T>A (CD300LF)	XP_011522673.1:p.Val278Asp
XM_011524372.1:c.797T>A (CD300LF)	XP_011522674.1:p.Val266Asp
XM_011524373.1:c.788T>A (CD300LF)	XP_011522675.1:p.Val263Asp
XM_011524374.1:c.788T>A (CD300LF)	XP_011522676.1:p.Val263Asp
XM_011524375.1:c.764T>A (CD300LF)	XP_011522677.1:p.Val255Asp
XM_011524376.1:c.*21T>A (CD300LF)	XP_011522678.1:n.*21T>A
XM_011524377.1:c.*21T>A (CD300LF)	XP_011522679.1:n.*21T>A
XM_011524378.1:c.*21T>A (CD300LF)	XP_011522680.1:n.*21T>A
XM_011524379.1:c.*21T>A (CD300LF)	XP_011522681.1:n.*21T>A
XM_017024212.2:c.767T>A (CD300LF)	XP_016879701.1:p.Val256Asp
XM_017024213.2:c.*21T>A (CD300LF)	XP_016879702.1:n.*21T>A
XM_017024214.2:c.*21T>A (CD300LF)	XP_016879703.1:n.*21T>A
XM_017024215.1:c.*21T>A (CD300LF)	XP_016879704.1:n.*21T>A
XM_017024216.2:c.*21T>A (CD300LF)	XP_016879705.1:n.*21T>A
XM_017024217.2:c.*21T>A (CD300LF)	XP_016879706.1:n.*21T>A
NM_139018.5:c.710T>A (CD300LF) MANE Select	NP_620587.2:p.Val237Asp
NM_001289082.2:c.*21T>A (CD300LF)	NP_001276011.1:n.*21T>A
NM_001289083.2:c.*21T>A (CD300LF)	NP_001276012.1:n.*21T>A
NM_001289084.2:c.755T>A (CD300LF)	NP_001276013.1:p.Val252Asp
NM_001289085.2:c.719T>A (CD300LF)	NP_001276014.1:p.Val240Asp
NM_001289086.2:c.*21T>A (CD300LF)	NP_001276015.1:n.*21T>A
NM_001289087.2:c.*21T>A (CD300LF)	NP_001276016.1:n.*21T>A
NM_175738.5:c.72+24074A>T (RAB37)	NP_783865.1:n.72+24074A>T
NR_110298.2:n.805T>A (CD300LF)