Canonical Allele Identifier: CA400935196
Gene: CD300LF HGNC NCBI
RAB37 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74695840C>T , CM000679.2:g.74695840C>T GRCh38
NC_000017.10:g.72691979C>T , CM000679.1:g.72691979C>T GRCh37
NC_000017.9:g.70203574C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326165.11:c.602G>A (CD300LF) MANE Select ENSP00000327075.6:p.Gly201Asp
ENST00000301573.13:c.648G>A (CD300LF) ENSP00000301573.9:p.Gly216=
ENST00000326165.10:c.602G>A (CD300LF) ENSP00000327075.6:p.Gly201Asp
ENST00000340415.7:c.72+24182C>T (RAB37) ENSP00000341354.3:n.72+24182C>T
ENST00000343125.8:c.498G>A (CD300LF) ENSP00000343751.4:p.Gly166=
ENST00000361254.8:c.633G>A (CD300LF) ENSP00000355294.4:p.Gly211=
ENST00000392617.7:n.479+24182C>T (RAB37)
ENST00000402449.8:c.72+24182C>T (RAB37) ENSP00000383934.4:n.72+24182C>T
ENST00000462044.5:c.475G>A (CD300LF) ENSP00000464223.1:p.Ala159Thr
ENST00000464910.5:c.611G>A (CD300LF) ENSP00000464257.1:p.Gly204Asp
ENST00000469092.5:c.498G>A (CD300LF) ENSP00000463743.1:p.Gly166=
ENST00000581500.1:c.633G>A (CD300LF) ENSP00000464610.1:p.Gly211=
ENST00000583937.5:c.647G>A (CD300LF) ENSP00000462309.1:p.Gly216Asp
NM_001289082.1:c.498G>A (CD300LF) NP_001276011.1:p.Gly166=
NM_001289083.1:c.648G>A (CD300LF) NP_001276012.1:p.Gly216=
NM_001289084.1:c.647G>A (CD300LF) NP_001276013.1:p.Gly216Asp
NM_001289085.1:c.611G>A (CD300LF) NP_001276014.1:p.Gly204Asp
NM_001289086.1:c.633G>A (CD300LF) NP_001276015.1:p.Gly211=
NM_001289087.1:c.579G>A (CD300LF) NP_001276016.1:p.Gly193=
NM_139018.4:c.602G>A (CD300LF) NP_620587.2:p.Gly201Asp
NM_175738.4:c.72+24182C>T (RAB37) NP_783865.1:n.72+24182C>T
NR_110298.1:n.774G>A (CD300LF)
XM_011524369.1:c.734G>A (CD300LF) XP_011522671.1:p.Gly245Asp
XM_011524370.1:c.725G>A (CD300LF) XP_011522672.1:p.Gly242Asp
XM_011524371.1:c.725G>A (CD300LF) XP_011522673.1:p.Gly242Asp
XM_011524372.1:c.689G>A (CD300LF) XP_011522674.1:p.Gly230Asp
XM_011524373.1:c.680G>A (CD300LF) XP_011522675.1:p.Gly227Asp
XM_011524374.1:c.680G>A (CD300LF) XP_011522676.1:p.Gly227Asp
XM_011524375.1:c.656G>A (CD300LF) XP_011522677.1:p.Gly219Asp
XM_011524376.1:c.711G>A (CD300LF) XP_011522678.1:p.Gly237=
XM_011524377.1:c.711G>A (CD300LF) XP_011522679.1:p.Gly237=
XM_011524378.1:c.702G>A (CD300LF) XP_011522680.1:p.Gly234=
XM_011524379.1:c.666G>A (CD300LF) XP_011522681.1:p.Gly222=
XM_017024212.2:c.659G>A (CD300LF) XP_016879701.1:p.Gly220Asp
XM_017024213.2:c.714G>A (CD300LF) XP_016879702.1:p.Gly238=
XM_017024214.2:c.705G>A (CD300LF) XP_016879703.1:p.Gly235=
XM_017024215.1:c.657G>A (CD300LF) XP_016879704.1:p.Gly219=
XM_017024216.2:c.636G>A (CD300LF) XP_016879705.1:p.Gly212=
XM_017024217.2:c.624G>A (CD300LF) XP_016879706.1:p.Gly208=
NM_139018.5:c.602G>A (CD300LF) MANE Select NP_620587.2:p.Gly201Asp
NM_001289082.2:c.498G>A (CD300LF) NP_001276011.1:p.Gly166=
NM_001289083.2:c.648G>A (CD300LF) NP_001276012.1:p.Gly216=
NM_001289084.2:c.647G>A (CD300LF) NP_001276013.1:p.Gly216Asp
NM_001289085.2:c.611G>A (CD300LF) NP_001276014.1:p.Gly204Asp
NM_001289086.2:c.633G>A (CD300LF) NP_001276015.1:p.Gly211=
NM_001289087.2:c.579G>A (CD300LF) NP_001276016.1:p.Gly193=
NM_175738.5:c.72+24182C>T (RAB37) NP_783865.1:n.72+24182C>T
NR_110298.2:n.697G>A (CD300LF)