Canonical Allele Identifier: CA371795746

Gene: VPS13B COX6C

Linked Data

• ClinVar Variation Id: 1955123
• ClinVar RCV Id: RCV002690455
• MyVariant Identifiers: chr8:g.100887750A>C (hg19) ; chr8:g.99875522A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99875522A>C , CM000670.2:g.99875522A>C	GRCh38
NC_000008.10:g.100887750A>C , CM000670.1:g.100887750A>C	GRCh37
NC_000008.9:g.100956926A>C	NCBI36
NG_007098.2:g.867257A>C , LRG_351:g.867257A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*1579A>C (VPS13B)	ENSP00000507923.1:n.*1579A>C
ENST00000682358.1:n.12555A>C (VPS13B)
ENST00000683334.1:c.*7607A>C (VPS13B)	ENSP00000507369.1:n.*7607A>C
ENST00000357162.7:c.11850A>C (VPS13B) MANE Select	ENSP00000349685.2:p.Gln3950His
ENST00000358544.7:c.11925A>C (VPS13B) MANE Plus Clinical	ENSP00000351346.2:p.Gln3975His
ENST00000357162.6:c.11850A>C (VPS13B)	ENSP00000349685.2:p.Gln3950His
ENST00000358544.6:c.11925A>C (VPS13B)	ENSP00000351346.2:p.Gln3975His
ENST00000493587.1:n.1427A>C (VPS13B)
ENST00000520517.5:c.*142-430T>G (COX6C)	ENSP00000429991.1:n.*142-430T>G
ENST00000522934.5:c.*142-2229T>G (COX6C)	ENSP00000428702.1:n.*142-2229T>G
NM_017890.4:c.11925A>C , LRG_351t1:c.11925A>C (VPS13B)	NP_060360.3:p.Gln3975His
NM_152564.4:c.11850A>C , LRG_351t2:c.11850A>C (VPS13B)	NP_689777.3:p.Gln3950His
XM_005250800.2:c.11925A>C (VPS13B)	XP_005250857.1:p.Gln3975His
XM_005250801.3:c.11925A>C (VPS13B)	XP_005250858.1:p.Gln3975His
XM_011516848.1:c.11922A>C (VPS13B)	XP_011515150.1:p.Gln3974His
XM_011516849.1:c.11847A>C (VPS13B)	XP_011515151.1:p.Gln3949His
XM_011516850.1:c.11547A>C (VPS13B)	XP_011515152.1:p.Gln3849His
XM_011516851.1:c.8811A>C (VPS13B)	XP_011515153.1:p.Gln2937His
XM_011516852.1:c.8811A>C (VPS13B)	XP_011515154.1:p.Gln2937His
XM_011516854.1:c.7704A>C (VPS13B)	XP_011515156.1:p.Gln2568His
XM_005250800.3:c.11925A>C (VPS13B)	XP_005250857.1:p.Gln3975His
XM_005250801.5:c.11925A>C (VPS13B)	XP_005250858.1:p.Gln3975His
XM_011516848.2:c.11922A>C (VPS13B)	XP_011515150.1:p.Gln3974His
XM_011516849.2:c.11847A>C (VPS13B)	XP_011515151.1:p.Gln3949His
XM_011516850.2:c.11547A>C (VPS13B)	XP_011515152.1:p.Gln3849His
XM_011516851.2:c.8811A>C (VPS13B)	XP_011515153.1:p.Gln2937His
XM_011516852.2:c.8811A>C (VPS13B)	XP_011515154.1:p.Gln2937His
XM_011516854.2:c.7704A>C (VPS13B)	XP_011515156.1:p.Gln2568His
XM_017013109.1:c.11730A>C (VPS13B)	XP_016868598.1:p.Gln3910His
XM_017013111.1:c.8811A>C (VPS13B)	XP_016868600.1:p.Gln2937His
XM_017013112.1:c.7482A>C (VPS13B)	XP_016868601.1:p.Gln2494His
XM_024447074.1:c.10710A>C (VPS13B)	XP_024302842.1:p.Gln3570His
NM_017890.5:c.11925A>C (VPS13B) MANE Plus Clinical	NP_060360.3:p.Gln3975His
NM_152564.5:c.11850A>C (VPS13B) MANE Select	NP_689777.3:p.Gln3950His