Canonical Allele Identifier: CA1708241

Gene: EXOC6B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72184095A>G , CM000664.2:g.72184095A>G	GRCh38
NC_000002.11:g.72411224A>G , CM000664.1:g.72411224A>G	GRCh37
NC_000002.10:g.72264732A>G	NCBI36
NG_050967.1:g.646954T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272427.11:c.2289T>C MANE Select	ENSP00000272427.7:p.Thr763=
ENST00000272427.10:c.2289T>C	ENSP00000272427.6:p.Thr763=
ENST00000471335.5:n.210T>C
ENST00000490919.5:n.228T>C
ENST00000492257.1:n.253T>C
ENST00000634650.1:c.2289T>C	ENSP00000489442.1:p.Thr763=
NM_015189.1:c.2289T>C	NP_056004.1:p.Thr763=
XM_005264223.1:c.2289T>C	XP_005264280.1:p.Thr763=
XM_005264224.1:c.1293T>C	XP_005264281.1:p.Thr431=
XM_011532710.1:c.2220T>C	XP_011531012.1:p.Thr740=
NM_001321729.1:c.2289T>C	NP_001308658.1:p.Thr763=
NM_001321730.1:c.2154T>C	NP_001308659.1:p.Thr718=
NM_001321731.1:c.2289T>C	NP_001308660.1:p.Thr763=
NM_001321733.1:c.2154T>C	NP_001308662.1:p.Thr718=
NM_001321734.1:c.1950T>C	NP_001308663.1:p.Thr650=
NM_015189.2:c.2289T>C	NP_056004.1:p.Thr763=
NR_135773.1:n.2347T>C
NR_135774.1:n.2099T>C
XM_017003641.1:c.1743T>C	XP_016859130.1:p.Thr581=
XM_017003642.1:c.1293T>C	XP_016859131.1:p.Thr431=
NM_001321729.2:c.2289T>C	NP_001308658.1:p.Thr763=
NM_001321730.2:c.2154T>C	NP_001308659.1:p.Thr718=
NM_001321731.2:c.2289T>C	NP_001308660.1:p.Thr763=
NM_001321733.2:c.2154T>C	NP_001308662.1:p.Thr718=
NM_001321734.2:c.1950T>C	NP_001308663.1:p.Thr650=
NM_015189.3:c.2289T>C MANE Select	NP_056004.1:p.Thr763=
NR_135773.2:n.2338T>C
NR_135774.2:n.2090T>C