Canonical Allele Identifier: CA1260398777

Gene: EXOC6B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72184019A>C , CM000664.2:g.72184019A>C	GRCh38
NC_000002.11:g.72411148A>C , CM000664.1:g.72411148A>C	GRCh37
NC_000002.10:g.72264656A>C	NCBI36
NG_050967.1:g.647030T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015189.3:c.2309+56T>G MANE Select	NP_056004.1:n.2309+56T>G
ENST00000272427.11:c.2309+56T>G MANE Select	ENSP00000272427.7:n.2309+56T>G
NM_001321729.1:c.2309+56T>G	NP_001308658.1:n.2309+56T>G
NM_001321729.2:c.2309+56T>G	NP_001308658.1:n.2309+56T>G
NM_001321730.1:c.2174+56T>G	NP_001308659.1:n.2174+56T>G
NM_001321730.2:c.2174+56T>G	NP_001308659.1:n.2174+56T>G
NM_001321731.1:c.2309+56T>G	NP_001308660.1:n.2309+56T>G
NM_001321731.2:c.2309+56T>G	NP_001308660.1:n.2309+56T>G
NM_001321733.1:c.2174+56T>G	NP_001308662.1:n.2174+56T>G
NM_001321733.2:c.2174+56T>G	NP_001308662.1:n.2174+56T>G
NM_001321734.1:c.1970+56T>G	NP_001308663.1:n.1970+56T>G
NM_001321734.2:c.1970+56T>G	NP_001308663.1:n.1970+56T>G
NM_015189.1:c.2309+56T>G	NP_056004.1:n.2309+56T>G
NM_015189.2:c.2309+56T>G	NP_056004.1:n.2309+56T>G
NR_135773.1:n.2367+56T>G
NR_135773.2:n.2358+56T>G
NR_135774.1:n.2119+56T>G
NR_135774.2:n.2110+56T>G
ENST00000272427.10:c.2309+56T>G	ENSP00000272427.6:n.2309+56T>G
ENST00000471335.5:n.230+56T>G
ENST00000490919.5:n.248+56T>G
ENST00000492257.1:n.273+56T>G
ENST00000634650.1:c.2309+56T>G	ENSP00000489442.1:n.2309+56T>G
XM_005264223.1:c.2309+56T>G	XP_005264280.1:n.2309+56T>G
XM_005264224.1:c.1313+56T>G	XP_005264281.1:n.1313+56T>G
XM_011532710.1:c.2240+56T>G	XP_011531012.1:n.2240+56T>G
XM_017003641.1:c.1763+56T>G	XP_016859130.1:n.1763+56T>G
XM_017003642.1:c.1313+56T>G	XP_016859131.1:n.1313+56T>G