Canonical Allele Identifier: CA400935162

Gene: CD300LF RAB37

Linked Data

• MyVariant Identifiers: chr17:g.72691966A>C (hg19) ; chr17:g.74695827A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74695827A>C , CM000679.2:g.74695827A>C	GRCh38
NC_000017.10:g.72691966A>C , CM000679.1:g.72691966A>C	GRCh37
NC_000017.9:g.70203561A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326165.11:c.615T>G (CD300LF) MANE Select	ENSP00000327075.6:p.Tyr205Ter
ENST00000301573.13:c.661T>G (CD300LF)	ENSP00000301573.9:p.Cys221Gly
ENST00000326165.10:c.615T>G (CD300LF)	ENSP00000327075.6:p.Tyr205Ter
ENST00000340415.7:c.72+24169A>C (RAB37)	ENSP00000341354.3:n.72+24169A>C
ENST00000343125.8:c.511T>G (CD300LF)	ENSP00000343751.4:p.Cys171Gly
ENST00000361254.8:c.646T>G (CD300LF)	ENSP00000355294.4:p.Cys216Gly
ENST00000392617.7:n.479+24169A>C (RAB37)
ENST00000402449.8:c.72+24169A>C (RAB37)	ENSP00000383934.4:n.72+24169A>C
ENST00000462044.5:c.488T>G (CD300LF)	ENSP00000464223.1:p.Met163Arg
ENST00000464910.5:c.624T>G (CD300LF)	ENSP00000464257.1:p.Tyr208Ter
ENST00000469092.5:c.511T>G (CD300LF)	ENSP00000463743.1:p.Cys171Gly
ENST00000581500.1:c.646T>G (CD300LF)	ENSP00000464610.1:p.Cys216Gly
ENST00000583937.5:c.660T>G (CD300LF)	ENSP00000462309.1:p.Tyr220Ter
NM_001289082.1:c.511T>G (CD300LF)	NP_001276011.1:p.Cys171Gly
NM_001289083.1:c.661T>G (CD300LF)	NP_001276012.1:p.Cys221Gly
NM_001289084.1:c.660T>G (CD300LF)	NP_001276013.1:p.Tyr220Ter
NM_001289085.1:c.624T>G (CD300LF)	NP_001276014.1:p.Tyr208Ter
NM_001289086.1:c.646T>G (CD300LF)	NP_001276015.1:p.Cys216Gly
NM_001289087.1:c.592T>G (CD300LF)	NP_001276016.1:p.Cys198Gly
NM_139018.4:c.615T>G (CD300LF)	NP_620587.2:p.Tyr205Ter
NM_175738.4:c.72+24169A>C (RAB37)	NP_783865.1:n.72+24169A>C
NR_110298.1:n.787T>G (CD300LF)
XM_011524369.1:c.747T>G (CD300LF)	XP_011522671.1:p.Tyr249Ter
XM_011524370.1:c.738T>G (CD300LF)	XP_011522672.1:p.Tyr246Ter
XM_011524371.1:c.738T>G (CD300LF)	XP_011522673.1:p.Tyr246Ter
XM_011524372.1:c.702T>G (CD300LF)	XP_011522674.1:p.Tyr234Ter
XM_011524373.1:c.693T>G (CD300LF)	XP_011522675.1:p.Tyr231Ter
XM_011524374.1:c.693T>G (CD300LF)	XP_011522676.1:p.Tyr231Ter
XM_011524375.1:c.669T>G (CD300LF)	XP_011522677.1:p.Tyr223Ter
XM_011524376.1:c.724T>G (CD300LF)	XP_011522678.1:p.Cys242Gly
XM_011524377.1:c.724T>G (CD300LF)	XP_011522679.1:p.Cys242Gly
XM_011524378.1:c.715T>G (CD300LF)	XP_011522680.1:p.Cys239Gly
XM_011524379.1:c.679T>G (CD300LF)	XP_011522681.1:p.Cys227Gly
XM_017024212.2:c.672T>G (CD300LF)	XP_016879701.1:p.Tyr224Ter
XM_017024213.2:c.727T>G (CD300LF)	XP_016879702.1:p.Cys243Gly
XM_017024214.2:c.718T>G (CD300LF)	XP_016879703.1:p.Cys240Gly
XM_017024215.1:c.670T>G (CD300LF)	XP_016879704.1:p.Cys224Gly
XM_017024216.2:c.649T>G (CD300LF)	XP_016879705.1:p.Cys217Gly
XM_017024217.2:c.637T>G (CD300LF)	XP_016879706.1:p.Cys213Gly
NM_139018.5:c.615T>G (CD300LF) MANE Select	NP_620587.2:p.Tyr205Ter
NM_001289082.2:c.511T>G (CD300LF)	NP_001276011.1:p.Cys171Gly
NM_001289083.2:c.661T>G (CD300LF)	NP_001276012.1:p.Cys221Gly
NM_001289084.2:c.660T>G (CD300LF)	NP_001276013.1:p.Tyr220Ter
NM_001289085.2:c.624T>G (CD300LF)	NP_001276014.1:p.Tyr208Ter
NM_001289086.2:c.646T>G (CD300LF)	NP_001276015.1:p.Cys216Gly
NM_001289087.2:c.592T>G (CD300LF)	NP_001276016.1:p.Cys198Gly
NM_175738.5:c.72+24169A>C (RAB37)	NP_783865.1:n.72+24169A>C
NR_110298.2:n.710T>G (CD300LF)