Canonical Allele Identifier: CA1708521

Gene: EXOC6B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72499934C>T , CM000664.2:g.72499934C>T	GRCh38
NC_000002.11:g.72727063C>T , CM000664.1:g.72727063C>T	GRCh37
NC_000002.10:g.72580571C>T	NCBI36
NG_050967.1:g.331115G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272427.11:c.1206G>A MANE Select	ENSP00000272427.7:p.Lys402=
ENST00000272427.10:c.1206G>A	ENSP00000272427.6:p.Lys402=
ENST00000410104.1:c.1206G>A	ENSP00000386698.1:p.Lys402=
ENST00000410112.6:c.*917G>A	ENSP00000386634.2:n.*917G>A
ENST00000485398.1:n.610G>A
ENST00000634650.1:c.1206G>A	ENSP00000489442.1:p.Lys402=
NM_015189.1:c.1206G>A	NP_056004.1:p.Lys402=
XM_005264223.1:c.1206G>A	XP_005264280.1:p.Lys402=
XM_005264224.1:c.210G>A	XP_005264281.1:p.Lys70=
XM_011532710.1:c.1137G>A	XP_011531012.1:p.Lys379=
XM_011532711.1:c.1206G>A	XP_011531013.1:p.Lys402=
XM_011532712.1:c.1206G>A	XP_011531014.1:p.Lys402=
NM_001321729.1:c.1206G>A	NP_001308658.1:p.Lys402=
NM_001321730.1:c.1206G>A	NP_001308659.1:p.Lys402=
NM_001321731.1:c.1206G>A	NP_001308660.1:p.Lys402=
NM_001321733.1:c.1206G>A	NP_001308662.1:p.Lys402=
NM_001321734.1:c.867G>A	NP_001308663.1:p.Lys289=
NM_015189.2:c.1206G>A	NP_056004.1:p.Lys402=
NR_135773.1:n.1338G>A
NR_135774.1:n.1338G>A
XM_011532711.3:c.1206G>A	XP_011531013.1:p.Lys402=
XM_011532712.3:c.1206G>A	XP_011531014.1:p.Lys402=
XM_017003641.1:c.660G>A	XP_016859130.1:p.Lys220=
XM_017003642.1:c.210G>A	XP_016859131.1:p.Lys70=
NM_001321729.2:c.1206G>A	NP_001308658.1:p.Lys402=
NM_001321730.2:c.1206G>A	NP_001308659.1:p.Lys402=
NM_001321731.2:c.1206G>A	NP_001308660.1:p.Lys402=
NM_001321733.2:c.1206G>A	NP_001308662.1:p.Lys402=
NM_001321734.2:c.867G>A	NP_001308663.1:p.Lys289=
NM_015189.3:c.1206G>A MANE Select	NP_056004.1:p.Lys402=
NR_135773.2:n.1329G>A
NR_135774.2:n.1329G>A