Canonical Allele Identifier: CA1708403

Gene: EXOC6B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72492402C>A , CM000664.2:g.72492402C>A	GRCh38
NC_000002.11:g.72719531C>A , CM000664.1:g.72719531C>A	GRCh37
NC_000002.10:g.72573039C>A	NCBI36
NG_050967.1:g.338647G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272427.11:c.1581G>T MANE Select	ENSP00000272427.7:p.Arg527=
ENST00000272427.10:c.1581G>T	ENSP00000272427.6:p.Arg527=
ENST00000410104.1:c.1581G>T	ENSP00000386698.1:p.Arg527=
ENST00000464347.2:n.138G>T
ENST00000634650.1:c.1581G>T	ENSP00000489442.1:p.Arg527=
NM_015189.1:c.1581G>T	NP_056004.1:p.Arg527=
XM_005264223.1:c.1581G>T	XP_005264280.1:p.Arg527=
XM_005264224.1:c.585G>T	XP_005264281.1:p.Arg195=
XM_011532710.1:c.1512G>T	XP_011531012.1:p.Arg504=
XM_011532711.1:c.1581G>T	XP_011531013.1:p.Arg527=
XM_011532712.1:c.1581G>T	XP_011531014.1:p.Arg527=
NM_001321729.1:c.1581G>T	NP_001308658.1:p.Arg527=
NM_001321730.1:c.1581G>T	NP_001308659.1:p.Arg527=
NM_001321731.1:c.1581G>T	NP_001308660.1:p.Arg527=
NM_001321733.1:c.1581G>T	NP_001308662.1:p.Arg527=
NM_001321734.1:c.1242G>T	NP_001308663.1:p.Arg414=
NM_015189.2:c.1581G>T	NP_056004.1:p.Arg527=
NR_135773.1:n.1713G>T
NR_135774.1:n.1713G>T
XM_011532711.3:c.1581G>T	XP_011531013.1:p.Arg527=
XM_011532712.3:c.1581G>T	XP_011531014.1:p.Arg527=
XM_017003641.1:c.1035G>T	XP_016859130.1:p.Arg345=
XM_017003642.1:c.585G>T	XP_016859131.1:p.Arg195=
NM_001321729.2:c.1581G>T	NP_001308658.1:p.Arg527=
NM_001321730.2:c.1581G>T	NP_001308659.1:p.Arg527=
NM_001321731.2:c.1581G>T	NP_001308660.1:p.Arg527=
NM_001321733.2:c.1581G>T	NP_001308662.1:p.Arg527=
NM_001321734.2:c.1242G>T	NP_001308663.1:p.Arg414=
NM_015189.3:c.1581G>T MANE Select	NP_056004.1:p.Arg527=
NR_135773.2:n.1704G>T
NR_135774.2:n.1704G>T