Canonical Allele Identifier: CA400935042

Gene: CD300LF RAB37

Linked Data

• MyVariant Identifiers: chr17:g.72691921A>G (hg19) ; chr17:g.74695782A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74695782A>G , CM000679.2:g.74695782A>G	GRCh38
NC_000017.10:g.72691921A>G , CM000679.1:g.72691921A>G	GRCh37
NC_000017.9:g.70203516A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326165.11:c.660T>C (CD300LF) MANE Select	ENSP00000327075.6:p.Ala220=
ENST00000301573.13:c.706T>C (CD300LF)	ENSP00000301573.9:p.Tyr236His
ENST00000326165.10:c.660T>C (CD300LF)	ENSP00000327075.6:p.Ala220=
ENST00000340415.7:c.72+24124A>G (RAB37)	ENSP00000341354.3:n.72+24124A>G
ENST00000343125.8:c.556T>C (CD300LF)	ENSP00000343751.4:p.Tyr186His
ENST00000361254.8:c.691T>C (CD300LF)	ENSP00000355294.4:p.Tyr231His
ENST00000392617.7:n.479+24124A>G (RAB37)
ENST00000402449.8:c.72+24124A>G (RAB37)	ENSP00000383934.4:n.72+24124A>G
ENST00000462044.5:c.*35T>C (CD300LF)	ENSP00000464223.1:n.*35T>C
ENST00000464910.5:c.669T>C (CD300LF)	ENSP00000464257.1:p.Ala223=
ENST00000469092.5:c.556T>C (CD300LF)	ENSP00000463743.1:p.Tyr186His
ENST00000581500.1:c.691T>C (CD300LF)	ENSP00000464610.1:p.Tyr231His
ENST00000583937.5:c.705T>C (CD300LF)	ENSP00000462309.1:p.Ala235=
NM_001289082.1:c.556T>C (CD300LF)	NP_001276011.1:p.Tyr186His
NM_001289083.1:c.706T>C (CD300LF)	NP_001276012.1:p.Tyr236His
NM_001289084.1:c.705T>C (CD300LF)	NP_001276013.1:p.Ala235=
NM_001289085.1:c.669T>C (CD300LF)	NP_001276014.1:p.Ala223=
NM_001289086.1:c.691T>C (CD300LF)	NP_001276015.1:p.Tyr231His
NM_001289087.1:c.637T>C (CD300LF)	NP_001276016.1:p.Tyr213His
NM_139018.4:c.660T>C (CD300LF)	NP_620587.2:p.Ala220=
NM_175738.4:c.72+24124A>G (RAB37)	NP_783865.1:n.72+24124A>G
NR_110298.1:n.832T>C (CD300LF)
XM_011524369.1:c.792T>C (CD300LF)	XP_011522671.1:p.Ala264=
XM_011524370.1:c.783T>C (CD300LF)	XP_011522672.1:p.Ala261=
XM_011524371.1:c.783T>C (CD300LF)	XP_011522673.1:p.Ala261=
XM_011524372.1:c.747T>C (CD300LF)	XP_011522674.1:p.Ala249=
XM_011524373.1:c.738T>C (CD300LF)	XP_011522675.1:p.Ala246=
XM_011524374.1:c.738T>C (CD300LF)	XP_011522676.1:p.Ala246=
XM_011524375.1:c.714T>C (CD300LF)	XP_011522677.1:p.Ala238=
XM_011524376.1:c.769T>C (CD300LF)	XP_011522678.1:p.Tyr257His
XM_011524377.1:c.769T>C (CD300LF)	XP_011522679.1:p.Tyr257His
XM_011524378.1:c.760T>C (CD300LF)	XP_011522680.1:p.Tyr254His
XM_011524379.1:c.724T>C (CD300LF)	XP_011522681.1:p.Tyr242His
XM_017024212.2:c.717T>C (CD300LF)	XP_016879701.1:p.Ala239=
XM_017024213.2:c.772T>C (CD300LF)	XP_016879702.1:p.Tyr258His
XM_017024214.2:c.763T>C (CD300LF)	XP_016879703.1:p.Tyr255His
XM_017024215.1:c.715T>C (CD300LF)	XP_016879704.1:p.Tyr239His
XM_017024216.2:c.694T>C (CD300LF)	XP_016879705.1:p.Tyr232His
XM_017024217.2:c.682T>C (CD300LF)	XP_016879706.1:p.Tyr228His
NM_139018.5:c.660T>C (CD300LF) MANE Select	NP_620587.2:p.Ala220=
NM_001289082.2:c.556T>C (CD300LF)	NP_001276011.1:p.Tyr186His
NM_001289083.2:c.706T>C (CD300LF)	NP_001276012.1:p.Tyr236His
NM_001289084.2:c.705T>C (CD300LF)	NP_001276013.1:p.Ala235=
NM_001289085.2:c.669T>C (CD300LF)	NP_001276014.1:p.Ala223=
NM_001289086.2:c.691T>C (CD300LF)	NP_001276015.1:p.Tyr231His
NM_001289087.2:c.637T>C (CD300LF)	NP_001276016.1:p.Tyr213His
NM_175738.5:c.72+24124A>G (RAB37)	NP_783865.1:n.72+24124A>G
NR_110298.2:n.755T>C (CD300LF)