Canonical Allele Identifier: CA2275147035
Gene: CD300LF HGNC NCBI
RAB37 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74695826C= , CM000679.2:g.74695826C= GRCh38
NC_000017.10:g.72691965C= , CM000679.1:g.72691965C= GRCh37
NC_000017.9:g.70203560C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326165.11:c.616G= (CD300LF) MANE Select ENSP00000327075.6:p.Ala206=
ENST00000301573.13:c.662G= (CD300LF) ENSP00000301573.9:p.Cys221=
ENST00000326165.10:c.616G= (CD300LF) ENSP00000327075.6:p.Ala206=
ENST00000340415.7:c.72+24168C= (RAB37) ENSP00000341354.3:n.72+24168C=
ENST00000343125.8:c.512G= (CD300LF) ENSP00000343751.4:p.Cys171=
ENST00000361254.8:c.647G= (CD300LF) ENSP00000355294.4:p.Cys216=
ENST00000392617.7:n.479+24168C= (RAB37)
ENST00000402449.8:c.72+24168C= (RAB37) ENSP00000383934.4:n.72+24168C=
ENST00000462044.5:c.489G= (CD300LF) ENSP00000464223.1:p.Met163=
ENST00000464910.5:c.625G= (CD300LF) ENSP00000464257.1:p.Ala209=
ENST00000469092.5:c.512G= (CD300LF) ENSP00000463743.1:p.Cys171=
ENST00000581500.1:c.647G= (CD300LF) ENSP00000464610.1:p.Cys216=
ENST00000583937.5:c.661G= (CD300LF) ENSP00000462309.1:p.Ala221=
NM_001289082.1:c.512G= (CD300LF) NP_001276011.1:p.Cys171=
NM_001289083.1:c.662G= (CD300LF) NP_001276012.1:p.Cys221=
NM_001289084.1:c.661G= (CD300LF) NP_001276013.1:p.Ala221=
NM_001289085.1:c.625G= (CD300LF) NP_001276014.1:p.Ala209=
NM_001289086.1:c.647G= (CD300LF) NP_001276015.1:p.Cys216=
NM_001289087.1:c.593G= (CD300LF) NP_001276016.1:p.Cys198=
NM_139018.4:c.616G= (CD300LF) NP_620587.2:p.Ala206=
NM_175738.4:c.72+24168C= (RAB37) NP_783865.1:n.72+24168C=
NR_110298.1:n.788G= (CD300LF)
XM_011524369.1:c.748G= (CD300LF) XP_011522671.1:p.Ala250=
XM_011524370.1:c.739G= (CD300LF) XP_011522672.1:p.Ala247=
XM_011524371.1:c.739G= (CD300LF) XP_011522673.1:p.Ala247=
XM_011524372.1:c.703G= (CD300LF) XP_011522674.1:p.Ala235=
XM_011524373.1:c.694G= (CD300LF) XP_011522675.1:p.Ala232=
XM_011524374.1:c.694G= (CD300LF) XP_011522676.1:p.Ala232=
XM_011524375.1:c.670G= (CD300LF) XP_011522677.1:p.Ala224=
XM_011524376.1:c.725G= (CD300LF) XP_011522678.1:p.Cys242=
XM_011524377.1:c.725G= (CD300LF) XP_011522679.1:p.Cys242=
XM_011524378.1:c.716G= (CD300LF) XP_011522680.1:p.Cys239=
XM_011524379.1:c.680G= (CD300LF) XP_011522681.1:p.Cys227=
XM_017024212.2:c.673G= (CD300LF) XP_016879701.1:p.Ala225=
XM_017024213.2:c.728G= (CD300LF) XP_016879702.1:p.Cys243=
XM_017024214.2:c.719G= (CD300LF) XP_016879703.1:p.Cys240=
XM_017024215.1:c.671G= (CD300LF) XP_016879704.1:p.Cys224=
XM_017024216.2:c.650G= (CD300LF) XP_016879705.1:p.Cys217=
XM_017024217.2:c.638G= (CD300LF) XP_016879706.1:p.Cys213=
NM_139018.5:c.616G= (CD300LF) MANE Select NP_620587.2:p.Ala206=
NM_001289082.2:c.512G= (CD300LF) NP_001276011.1:p.Cys171=
NM_001289083.2:c.662G= (CD300LF) NP_001276012.1:p.Cys221=
NM_001289084.2:c.661G= (CD300LF) NP_001276013.1:p.Ala221=
NM_001289085.2:c.625G= (CD300LF) NP_001276014.1:p.Ala209=
NM_001289086.2:c.647G= (CD300LF) NP_001276015.1:p.Cys216=
NM_001289087.2:c.593G= (CD300LF) NP_001276016.1:p.Cys198=
NM_175738.5:c.72+24168C= (RAB37) NP_783865.1:n.72+24168C=
NR_110298.2:n.711G= (CD300LF)