Canonical Allele Identifier: CA1708244

Gene: EXOC6B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72184110C>T , CM000664.2:g.72184110C>T	GRCh38
NC_000002.11:g.72411239C>T , CM000664.1:g.72411239C>T	GRCh37
NC_000002.10:g.72264747C>T	NCBI36
NG_050967.1:g.646939G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272427.11:c.2274G>A MANE Select	ENSP00000272427.7:p.Arg758=
ENST00000272427.10:c.2274G>A	ENSP00000272427.6:p.Arg758=
ENST00000471335.5:n.195G>A
ENST00000490919.5:n.213G>A
ENST00000492257.1:n.238G>A
ENST00000634650.1:c.2274G>A	ENSP00000489442.1:p.Arg758=
NM_015189.1:c.2274G>A	NP_056004.1:p.Arg758=
XM_005264223.1:c.2274G>A	XP_005264280.1:p.Arg758=
XM_005264224.1:c.1278G>A	XP_005264281.1:p.Arg426=
XM_011532710.1:c.2205G>A	XP_011531012.1:p.Arg735=
NM_001321729.1:c.2274G>A	NP_001308658.1:p.Arg758=
NM_001321730.1:c.2139G>A	NP_001308659.1:p.Arg713=
NM_001321731.1:c.2274G>A	NP_001308660.1:p.Arg758=
NM_001321733.1:c.2139G>A	NP_001308662.1:p.Arg713=
NM_001321734.1:c.1935G>A	NP_001308663.1:p.Arg645=
NM_015189.2:c.2274G>A	NP_056004.1:p.Arg758=
NR_135773.1:n.2332G>A
NR_135774.1:n.2084G>A
XM_017003641.1:c.1728G>A	XP_016859130.1:p.Arg576=
XM_017003642.1:c.1278G>A	XP_016859131.1:p.Arg426=
NM_001321729.2:c.2274G>A	NP_001308658.1:p.Arg758=
NM_001321730.2:c.2139G>A	NP_001308659.1:p.Arg713=
NM_001321731.2:c.2274G>A	NP_001308660.1:p.Arg758=
NM_001321733.2:c.2139G>A	NP_001308662.1:p.Arg713=
NM_001321734.2:c.1935G>A	NP_001308663.1:p.Arg645=
NM_015189.3:c.2274G>A MANE Select	NP_056004.1:p.Arg758=
NR_135773.2:n.2323G>A
NR_135774.2:n.2075G>A