Canonical Allele Identifier: CA1708340

Gene: EXOC6B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72465247G>A , CM000664.2:g.72465247G>A	GRCh38
NC_000002.11:g.72692376G>A , CM000664.1:g.72692376G>A	GRCh37
NC_000002.10:g.72545884G>A	NCBI36
NG_050967.1:g.365802C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272427.11:c.1893C>T MANE Select	ENSP00000272427.7:p.Thr631=
ENST00000272427.10:c.1893C>T	ENSP00000272427.6:p.Thr631=
ENST00000410104.1:c.1893C>T	ENSP00000386698.1:p.Thr631=
ENST00000464347.2:n.315C>T
ENST00000634650.1:c.1893C>T	ENSP00000489442.1:p.Thr631=
NM_015189.1:c.1893C>T	NP_056004.1:p.Thr631=
XM_005264223.1:c.1893C>T	XP_005264280.1:p.Thr631=
XM_005264224.1:c.897C>T	XP_005264281.1:p.Thr299=
XM_011532710.1:c.1824C>T	XP_011531012.1:p.Thr608=
XM_011532711.1:c.1893C>T	XP_011531013.1:p.Thr631=
XM_011532712.1:c.1893C>T	XP_011531014.1:p.Thr631=
NM_001321729.1:c.1893C>T	NP_001308658.1:p.Thr631=
NM_001321730.1:c.1758C>T	NP_001308659.1:p.Thr586=
NM_001321731.1:c.1893C>T	NP_001308660.1:p.Thr631=
NM_001321733.1:c.1758C>T	NP_001308662.1:p.Thr586=
NM_001321734.1:c.1554C>T	NP_001308663.1:p.Thr518=
NM_015189.2:c.1893C>T	NP_056004.1:p.Thr631=
NR_135773.1:n.2025C>T
NR_135774.1:n.1932+15369C>T
XM_011532711.3:c.1893C>T	XP_011531013.1:p.Thr631=
XM_011532712.3:c.1893C>T	XP_011531014.1:p.Thr631=
XM_017003641.1:c.1347C>T	XP_016859130.1:p.Thr449=
XM_017003642.1:c.897C>T	XP_016859131.1:p.Thr299=
NM_001321729.2:c.1893C>T	NP_001308658.1:p.Thr631=
NM_001321730.2:c.1758C>T	NP_001308659.1:p.Thr586=
NM_001321731.2:c.1893C>T	NP_001308660.1:p.Thr631=
NM_001321733.2:c.1758C>T	NP_001308662.1:p.Thr586=
NM_001321734.2:c.1554C>T	NP_001308663.1:p.Thr518=
NM_015189.3:c.1893C>T MANE Select	NP_056004.1:p.Thr631=
NR_135773.2:n.2016C>T
NR_135774.2:n.1923+15369C>T