Canonical Allele Identifier: CA400935086

Gene: CD300LF RAB37

Linked Data

• MyVariant Identifiers: chr17:g.72691937G>C (hg19) ; chr17:g.74695798G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74695798G>C , CM000679.2:g.74695798G>C	GRCh38
NC_000017.10:g.72691937G>C , CM000679.1:g.72691937G>C	GRCh37
NC_000017.9:g.70203532G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326165.11:c.644C>G (CD300LF) MANE Select	ENSP00000327075.6:p.Thr215Ser
ENST00000301573.13:c.690C>G (CD300LF)	ENSP00000301573.9:p.Asn230Lys
ENST00000326165.10:c.644C>G (CD300LF)	ENSP00000327075.6:p.Thr215Ser
ENST00000340415.7:c.72+24140G>C (RAB37)	ENSP00000341354.3:n.72+24140G>C
ENST00000343125.8:c.540C>G (CD300LF)	ENSP00000343751.4:p.Asn180Lys
ENST00000361254.8:c.675C>G (CD300LF)	ENSP00000355294.4:p.Asn225Lys
ENST00000392617.7:n.479+24140G>C (RAB37)
ENST00000402449.8:c.72+24140G>C (RAB37)	ENSP00000383934.4:n.72+24140G>C
ENST00000462044.5:c.*19C>G (CD300LF)	ENSP00000464223.1:n.*19C>G
ENST00000464910.5:c.653C>G (CD300LF)	ENSP00000464257.1:p.Thr218Ser
ENST00000469092.5:c.540C>G (CD300LF)	ENSP00000463743.1:p.Asn180Lys
ENST00000581500.1:c.675C>G (CD300LF)	ENSP00000464610.1:p.Asn225Lys
ENST00000583937.5:c.689C>G (CD300LF)	ENSP00000462309.1:p.Thr230Ser
NM_001289082.1:c.540C>G (CD300LF)	NP_001276011.1:p.Asn180Lys
NM_001289083.1:c.690C>G (CD300LF)	NP_001276012.1:p.Asn230Lys
NM_001289084.1:c.689C>G (CD300LF)	NP_001276013.1:p.Thr230Ser
NM_001289085.1:c.653C>G (CD300LF)	NP_001276014.1:p.Thr218Ser
NM_001289086.1:c.675C>G (CD300LF)	NP_001276015.1:p.Asn225Lys
NM_001289087.1:c.621C>G (CD300LF)	NP_001276016.1:p.Asn207Lys
NM_139018.4:c.644C>G (CD300LF)	NP_620587.2:p.Thr215Ser
NM_175738.4:c.72+24140G>C (RAB37)	NP_783865.1:n.72+24140G>C
NR_110298.1:n.816C>G (CD300LF)
XM_011524369.1:c.776C>G (CD300LF)	XP_011522671.1:p.Thr259Ser
XM_011524370.1:c.767C>G (CD300LF)	XP_011522672.1:p.Thr256Ser
XM_011524371.1:c.767C>G (CD300LF)	XP_011522673.1:p.Thr256Ser
XM_011524372.1:c.731C>G (CD300LF)	XP_011522674.1:p.Thr244Ser
XM_011524373.1:c.722C>G (CD300LF)	XP_011522675.1:p.Thr241Ser
XM_011524374.1:c.722C>G (CD300LF)	XP_011522676.1:p.Thr241Ser
XM_011524375.1:c.698C>G (CD300LF)	XP_011522677.1:p.Thr233Ser
XM_011524376.1:c.753C>G (CD300LF)	XP_011522678.1:p.Asn251Lys
XM_011524377.1:c.753C>G (CD300LF)	XP_011522679.1:p.Asn251Lys
XM_011524378.1:c.744C>G (CD300LF)	XP_011522680.1:p.Asn248Lys
XM_011524379.1:c.708C>G (CD300LF)	XP_011522681.1:p.Asn236Lys
XM_017024212.2:c.701C>G (CD300LF)	XP_016879701.1:p.Thr234Ser
XM_017024213.2:c.756C>G (CD300LF)	XP_016879702.1:p.Asn252Lys
XM_017024214.2:c.747C>G (CD300LF)	XP_016879703.1:p.Asn249Lys
XM_017024215.1:c.699C>G (CD300LF)	XP_016879704.1:p.Asn233Lys
XM_017024216.2:c.678C>G (CD300LF)	XP_016879705.1:p.Asn226Lys
XM_017024217.2:c.666C>G (CD300LF)	XP_016879706.1:p.Asn222Lys
NM_139018.5:c.644C>G (CD300LF) MANE Select	NP_620587.2:p.Thr215Ser
NM_001289082.2:c.540C>G (CD300LF)	NP_001276011.1:p.Asn180Lys
NM_001289083.2:c.690C>G (CD300LF)	NP_001276012.1:p.Asn230Lys
NM_001289084.2:c.689C>G (CD300LF)	NP_001276013.1:p.Thr230Ser
NM_001289085.2:c.653C>G (CD300LF)	NP_001276014.1:p.Thr218Ser
NM_001289086.2:c.675C>G (CD300LF)	NP_001276015.1:p.Asn225Lys
NM_001289087.2:c.621C>G (CD300LF)	NP_001276016.1:p.Asn207Lys
NM_175738.5:c.72+24140G>C (RAB37)	NP_783865.1:n.72+24140G>C
NR_110298.2:n.739C>G (CD300LF)