Canonical Allele Identifier: CA371795785

Gene: VPS13B COX6C

Linked Data

• dbSNP Id: rs996333047
• MyVariant Identifiers: chr8:g.100887759C>G (hg19) ; chr8:g.99875531C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99875531C>G , CM000670.2:g.99875531C>G	GRCh38
NC_000008.10:g.100887759C>G , CM000670.1:g.100887759C>G	GRCh37
NC_000008.9:g.100956935C>G	NCBI36
NG_007098.2:g.867266C>G , LRG_351:g.867266C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*1588C>G (VPS13B)	ENSP00000507923.1:n.*1588C>G
ENST00000682358.1:n.12564C>G (VPS13B)
ENST00000683334.1:c.*7616C>G (VPS13B)	ENSP00000507369.1:n.*7616C>G
ENST00000357162.7:c.11859C>G (VPS13B) MANE Select	ENSP00000349685.2:p.Cys3953Trp
ENST00000358544.7:c.11934C>G (VPS13B) MANE Plus Clinical	ENSP00000351346.2:p.Cys3978Trp
ENST00000357162.6:c.11859C>G (VPS13B)	ENSP00000349685.2:p.Cys3953Trp
ENST00000358544.6:c.11934C>G (VPS13B)	ENSP00000351346.2:p.Cys3978Trp
ENST00000493587.1:n.1436C>G (VPS13B)
ENST00000520517.5:c.*142-439G>C (COX6C)	ENSP00000429991.1:n.*142-439G>C
ENST00000522934.5:c.*142-2238G>C (COX6C)	ENSP00000428702.1:n.*142-2238G>C
NM_017890.4:c.11934C>G , LRG_351t1:c.11934C>G (VPS13B)	NP_060360.3:p.Cys3978Trp
NM_152564.4:c.11859C>G , LRG_351t2:c.11859C>G (VPS13B)	NP_689777.3:p.Cys3953Trp
XM_005250800.2:c.11934C>G (VPS13B)	XP_005250857.1:p.Cys3978Trp
XM_005250801.3:c.11934C>G (VPS13B)	XP_005250858.1:p.Cys3978Trp
XM_011516848.1:c.11931C>G (VPS13B)	XP_011515150.1:p.Cys3977Trp
XM_011516849.1:c.11856C>G (VPS13B)	XP_011515151.1:p.Cys3952Trp
XM_011516850.1:c.11556C>G (VPS13B)	XP_011515152.1:p.Cys3852Trp
XM_011516851.1:c.8820C>G (VPS13B)	XP_011515153.1:p.Cys2940Trp
XM_011516852.1:c.8820C>G (VPS13B)	XP_011515154.1:p.Cys2940Trp
XM_011516854.1:c.7713C>G (VPS13B)	XP_011515156.1:p.Cys2571Trp
XM_005250800.3:c.11934C>G (VPS13B)	XP_005250857.1:p.Cys3978Trp
XM_005250801.5:c.11934C>G (VPS13B)	XP_005250858.1:p.Cys3978Trp
XM_011516848.2:c.11931C>G (VPS13B)	XP_011515150.1:p.Cys3977Trp
XM_011516849.2:c.11856C>G (VPS13B)	XP_011515151.1:p.Cys3952Trp
XM_011516850.2:c.11556C>G (VPS13B)	XP_011515152.1:p.Cys3852Trp
XM_011516851.2:c.8820C>G (VPS13B)	XP_011515153.1:p.Cys2940Trp
XM_011516852.2:c.8820C>G (VPS13B)	XP_011515154.1:p.Cys2940Trp
XM_011516854.2:c.7713C>G (VPS13B)	XP_011515156.1:p.Cys2571Trp
XM_017013109.1:c.11739C>G (VPS13B)	XP_016868598.1:p.Cys3913Trp
XM_017013111.1:c.8820C>G (VPS13B)	XP_016868600.1:p.Cys2940Trp
XM_017013112.1:c.7491C>G (VPS13B)	XP_016868601.1:p.Cys2497Trp
XM_024447074.1:c.10719C>G (VPS13B)	XP_024302842.1:p.Cys3573Trp
NM_017890.5:c.11934C>G (VPS13B) MANE Plus Clinical	NP_060360.3:p.Cys3978Trp
NM_152564.5:c.11859C>G (VPS13B) MANE Select	NP_689777.3:p.Cys3953Trp