Canonical Allele Identifier: CA400935047

Gene: CD300LF RAB37

Linked Data

• MyVariant Identifiers: chr17:g.72691922G>T (hg19) ; chr17:g.74695783G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74695783G>T , CM000679.2:g.74695783G>T	GRCh38
NC_000017.10:g.72691922G>T , CM000679.1:g.72691922G>T	GRCh37
NC_000017.9:g.70203517G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326165.11:c.659C>A (CD300LF) MANE Select	ENSP00000327075.6:p.Ala220Asp
ENST00000301573.13:c.705C>A (CD300LF)	ENSP00000301573.9:p.Gly235=
ENST00000326165.10:c.659C>A (CD300LF)	ENSP00000327075.6:p.Ala220Asp
ENST00000340415.7:c.72+24125G>T (RAB37)	ENSP00000341354.3:n.72+24125G>T
ENST00000343125.8:c.555C>A (CD300LF)	ENSP00000343751.4:p.Gly185=
ENST00000361254.8:c.690C>A (CD300LF)	ENSP00000355294.4:p.Gly230=
ENST00000392617.7:n.479+24125G>T (RAB37)
ENST00000402449.8:c.72+24125G>T (RAB37)	ENSP00000383934.4:n.72+24125G>T
ENST00000462044.5:c.*34C>A (CD300LF)	ENSP00000464223.1:n.*34C>A
ENST00000464910.5:c.668C>A (CD300LF)	ENSP00000464257.1:p.Ala223Asp
ENST00000469092.5:c.555C>A (CD300LF)	ENSP00000463743.1:p.Gly185=
ENST00000581500.1:c.690C>A (CD300LF)	ENSP00000464610.1:p.Gly230=
ENST00000583937.5:c.704C>A (CD300LF)	ENSP00000462309.1:p.Ala235Asp
NM_001289082.1:c.555C>A (CD300LF)	NP_001276011.1:p.Gly185=
NM_001289083.1:c.705C>A (CD300LF)	NP_001276012.1:p.Gly235=
NM_001289084.1:c.704C>A (CD300LF)	NP_001276013.1:p.Ala235Asp
NM_001289085.1:c.668C>A (CD300LF)	NP_001276014.1:p.Ala223Asp
NM_001289086.1:c.690C>A (CD300LF)	NP_001276015.1:p.Gly230=
NM_001289087.1:c.636C>A (CD300LF)	NP_001276016.1:p.Gly212=
NM_139018.4:c.659C>A (CD300LF)	NP_620587.2:p.Ala220Asp
NM_175738.4:c.72+24125G>T (RAB37)	NP_783865.1:n.72+24125G>T
NR_110298.1:n.831C>A (CD300LF)
XM_011524369.1:c.791C>A (CD300LF)	XP_011522671.1:p.Ala264Asp
XM_011524370.1:c.782C>A (CD300LF)	XP_011522672.1:p.Ala261Asp
XM_011524371.1:c.782C>A (CD300LF)	XP_011522673.1:p.Ala261Asp
XM_011524372.1:c.746C>A (CD300LF)	XP_011522674.1:p.Ala249Asp
XM_011524373.1:c.737C>A (CD300LF)	XP_011522675.1:p.Ala246Asp
XM_011524374.1:c.737C>A (CD300LF)	XP_011522676.1:p.Ala246Asp
XM_011524375.1:c.713C>A (CD300LF)	XP_011522677.1:p.Ala238Asp
XM_011524376.1:c.768C>A (CD300LF)	XP_011522678.1:p.Gly256=
XM_011524377.1:c.768C>A (CD300LF)	XP_011522679.1:p.Gly256=
XM_011524378.1:c.759C>A (CD300LF)	XP_011522680.1:p.Gly253=
XM_011524379.1:c.723C>A (CD300LF)	XP_011522681.1:p.Gly241=
XM_017024212.2:c.716C>A (CD300LF)	XP_016879701.1:p.Ala239Asp
XM_017024213.2:c.771C>A (CD300LF)	XP_016879702.1:p.Gly257=
XM_017024214.2:c.762C>A (CD300LF)	XP_016879703.1:p.Gly254=
XM_017024215.1:c.714C>A (CD300LF)	XP_016879704.1:p.Gly238=
XM_017024216.2:c.693C>A (CD300LF)	XP_016879705.1:p.Gly231=
XM_017024217.2:c.681C>A (CD300LF)	XP_016879706.1:p.Gly227=
NM_139018.5:c.659C>A (CD300LF) MANE Select	NP_620587.2:p.Ala220Asp
NM_001289082.2:c.555C>A (CD300LF)	NP_001276011.1:p.Gly185=
NM_001289083.2:c.705C>A (CD300LF)	NP_001276012.1:p.Gly235=
NM_001289084.2:c.704C>A (CD300LF)	NP_001276013.1:p.Ala235Asp
NM_001289085.2:c.668C>A (CD300LF)	NP_001276014.1:p.Ala223Asp
NM_001289086.2:c.690C>A (CD300LF)	NP_001276015.1:p.Gly230=
NM_001289087.2:c.636C>A (CD300LF)	NP_001276016.1:p.Gly212=
NM_175738.5:c.72+24125G>T (RAB37)	NP_783865.1:n.72+24125G>T
NR_110298.2:n.754C>A (CD300LF)