Canonical Allele Identifier: CA1708546

Gene: EXOC6B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72513222A>G , CM000664.2:g.72513222A>G	GRCh38
NC_000002.11:g.72740351A>G , CM000664.1:g.72740351A>G	GRCh37
NC_000002.10:g.72593859A>G	NCBI36
NG_050967.1:g.317827T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272427.11:c.1077T>C MANE Select	ENSP00000272427.7:p.His359=
ENST00000272427.10:c.1077T>C	ENSP00000272427.6:p.His359=
ENST00000410104.1:c.1077T>C	ENSP00000386698.1:p.His359=
ENST00000410112.6:c.*788T>C	ENSP00000386634.2:n.*788T>C
ENST00000485398.1:n.481T>C
ENST00000634650.1:c.1077T>C	ENSP00000489442.1:p.His359=
NM_015189.1:c.1077T>C	NP_056004.1:p.His359=
XM_005264223.1:c.1077T>C	XP_005264280.1:p.His359=
XM_005264224.1:c.81T>C	XP_005264281.1:p.His27=
XM_011532710.1:c.1008T>C	XP_011531012.1:p.His336=
XM_011532711.1:c.1077T>C	XP_011531013.1:p.His359=
XM_011532712.1:c.1077T>C	XP_011531014.1:p.His359=
NM_001321729.1:c.1077T>C	NP_001308658.1:p.His359=
NM_001321730.1:c.1077T>C	NP_001308659.1:p.His359=
NM_001321731.1:c.1077T>C	NP_001308660.1:p.His359=
NM_001321733.1:c.1077T>C	NP_001308662.1:p.His359=
NM_001321734.1:c.738T>C	NP_001308663.1:p.His246=
NM_015189.2:c.1077T>C	NP_056004.1:p.His359=
NR_135773.1:n.1209T>C
NR_135774.1:n.1209T>C
XM_011532711.3:c.1077T>C	XP_011531013.1:p.His359=
XM_011532712.3:c.1077T>C	XP_011531014.1:p.His359=
XM_017003641.1:c.531T>C	XP_016859130.1:p.His177=
XM_017003642.1:c.81T>C	XP_016859131.1:p.His27=
NM_001321729.2:c.1077T>C	NP_001308658.1:p.His359=
NM_001321730.2:c.1077T>C	NP_001308659.1:p.His359=
NM_001321731.2:c.1077T>C	NP_001308660.1:p.His359=
NM_001321733.2:c.1077T>C	NP_001308662.1:p.His359=
NM_001321734.2:c.738T>C	NP_001308663.1:p.His246=
NM_015189.3:c.1077T>C MANE Select	NP_056004.1:p.His359=
NR_135773.2:n.1200T>C
NR_135774.2:n.1200T>C