Canonical Allele Identifier: CA371795627

Gene: VPS13B COX6C

Linked Data

• MyVariant Identifiers: chr8:g.100887722A>G (hg19) ; chr8:g.99875494A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99875494A>G , CM000670.2:g.99875494A>G	GRCh38
NC_000008.10:g.100887722A>G , CM000670.1:g.100887722A>G	GRCh37
NC_000008.9:g.100956898A>G	NCBI36
NG_007098.2:g.867229A>G , LRG_351:g.867229A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*1551A>G (VPS13B)	ENSP00000507923.1:n.*1551A>G
ENST00000682358.1:n.12527A>G (VPS13B)
ENST00000683334.1:c.*7579A>G (VPS13B)	ENSP00000507369.1:n.*7579A>G
ENST00000357162.7:c.11822A>G (VPS13B) MANE Select	ENSP00000349685.2:p.His3941Arg
ENST00000358544.7:c.11897A>G (VPS13B) MANE Plus Clinical	ENSP00000351346.2:p.His3966Arg
ENST00000357162.6:c.11822A>G (VPS13B)	ENSP00000349685.2:p.His3941Arg
ENST00000358544.6:c.11897A>G (VPS13B)	ENSP00000351346.2:p.His3966Arg
ENST00000493587.1:n.1399A>G (VPS13B)
ENST00000520517.5:c.*142-402T>C (COX6C)	ENSP00000429991.1:n.*142-402T>C
ENST00000522934.5:c.*142-2201T>C (COX6C)	ENSP00000428702.1:n.*142-2201T>C
NM_017890.4:c.11897A>G , LRG_351t1:c.11897A>G (VPS13B)	NP_060360.3:p.His3966Arg
NM_152564.4:c.11822A>G , LRG_351t2:c.11822A>G (VPS13B)	NP_689777.3:p.His3941Arg
XM_005250800.2:c.11897A>G (VPS13B)	XP_005250857.1:p.His3966Arg
XM_005250801.3:c.11897A>G (VPS13B)	XP_005250858.1:p.His3966Arg
XM_011516848.1:c.11894A>G (VPS13B)	XP_011515150.1:p.His3965Arg
XM_011516849.1:c.11819A>G (VPS13B)	XP_011515151.1:p.His3940Arg
XM_011516850.1:c.11519A>G (VPS13B)	XP_011515152.1:p.His3840Arg
XM_011516851.1:c.8783A>G (VPS13B)	XP_011515153.1:p.His2928Arg
XM_011516852.1:c.8783A>G (VPS13B)	XP_011515154.1:p.His2928Arg
XM_011516854.1:c.7676A>G (VPS13B)	XP_011515156.1:p.His2559Arg
XM_005250800.3:c.11897A>G (VPS13B)	XP_005250857.1:p.His3966Arg
XM_005250801.5:c.11897A>G (VPS13B)	XP_005250858.1:p.His3966Arg
XM_011516848.2:c.11894A>G (VPS13B)	XP_011515150.1:p.His3965Arg
XM_011516849.2:c.11819A>G (VPS13B)	XP_011515151.1:p.His3940Arg
XM_011516850.2:c.11519A>G (VPS13B)	XP_011515152.1:p.His3840Arg
XM_011516851.2:c.8783A>G (VPS13B)	XP_011515153.1:p.His2928Arg
XM_011516852.2:c.8783A>G (VPS13B)	XP_011515154.1:p.His2928Arg
XM_011516854.2:c.7676A>G (VPS13B)	XP_011515156.1:p.His2559Arg
XM_017013109.1:c.11702A>G (VPS13B)	XP_016868598.1:p.His3901Arg
XM_017013111.1:c.8783A>G (VPS13B)	XP_016868600.1:p.His2928Arg
XM_017013112.1:c.7454A>G (VPS13B)	XP_016868601.1:p.His2485Arg
XM_024447074.1:c.10682A>G (VPS13B)	XP_024302842.1:p.His3561Arg
NM_017890.5:c.11897A>G (VPS13B) MANE Plus Clinical	NP_060360.3:p.His3966Arg
NM_152564.5:c.11822A>G (VPS13B) MANE Select	NP_689777.3:p.His3941Arg