Canonical Allele Identifier: CA371795731

Gene: VPS13B COX6C

Linked Data

• MyVariant Identifiers: chr8:g.100887747G>C (hg19) ; chr8:g.99875519G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99875519G>C , CM000670.2:g.99875519G>C	GRCh38
NC_000008.10:g.100887747G>C , CM000670.1:g.100887747G>C	GRCh37
NC_000008.9:g.100956923G>C	NCBI36
NG_007098.2:g.867254G>C , LRG_351:g.867254G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*1576G>C (VPS13B)	ENSP00000507923.1:n.*1576G>C
ENST00000682358.1:n.12552G>C (VPS13B)
ENST00000683334.1:c.*7604G>C (VPS13B)	ENSP00000507369.1:n.*7604G>C
ENST00000357162.7:c.11847G>C (VPS13B) MANE Select	ENSP00000349685.2:p.Met3949Ile
ENST00000358544.7:c.11922G>C (VPS13B) MANE Plus Clinical	ENSP00000351346.2:p.Met3974Ile
ENST00000357162.6:c.11847G>C (VPS13B)	ENSP00000349685.2:p.Met3949Ile
ENST00000358544.6:c.11922G>C (VPS13B)	ENSP00000351346.2:p.Met3974Ile
ENST00000493587.1:n.1424G>C (VPS13B)
ENST00000520517.5:c.*142-427C>G (COX6C)	ENSP00000429991.1:n.*142-427C>G
ENST00000522934.5:c.*142-2226C>G (COX6C)	ENSP00000428702.1:n.*142-2226C>G
NM_017890.4:c.11922G>C , LRG_351t1:c.11922G>C (VPS13B)	NP_060360.3:p.Met3974Ile
NM_152564.4:c.11847G>C , LRG_351t2:c.11847G>C (VPS13B)	NP_689777.3:p.Met3949Ile
XM_005250800.2:c.11922G>C (VPS13B)	XP_005250857.1:p.Met3974Ile
XM_005250801.3:c.11922G>C (VPS13B)	XP_005250858.1:p.Met3974Ile
XM_011516848.1:c.11919G>C (VPS13B)	XP_011515150.1:p.Met3973Ile
XM_011516849.1:c.11844G>C (VPS13B)	XP_011515151.1:p.Met3948Ile
XM_011516850.1:c.11544G>C (VPS13B)	XP_011515152.1:p.Met3848Ile
XM_011516851.1:c.8808G>C (VPS13B)	XP_011515153.1:p.Met2936Ile
XM_011516852.1:c.8808G>C (VPS13B)	XP_011515154.1:p.Met2936Ile
XM_011516854.1:c.7701G>C (VPS13B)	XP_011515156.1:p.Met2567Ile
XM_005250800.3:c.11922G>C (VPS13B)	XP_005250857.1:p.Met3974Ile
XM_005250801.5:c.11922G>C (VPS13B)	XP_005250858.1:p.Met3974Ile
XM_011516848.2:c.11919G>C (VPS13B)	XP_011515150.1:p.Met3973Ile
XM_011516849.2:c.11844G>C (VPS13B)	XP_011515151.1:p.Met3948Ile
XM_011516850.2:c.11544G>C (VPS13B)	XP_011515152.1:p.Met3848Ile
XM_011516851.2:c.8808G>C (VPS13B)	XP_011515153.1:p.Met2936Ile
XM_011516852.2:c.8808G>C (VPS13B)	XP_011515154.1:p.Met2936Ile
XM_011516854.2:c.7701G>C (VPS13B)	XP_011515156.1:p.Met2567Ile
XM_017013109.1:c.11727G>C (VPS13B)	XP_016868598.1:p.Met3909Ile
XM_017013111.1:c.8808G>C (VPS13B)	XP_016868600.1:p.Met2936Ile
XM_017013112.1:c.7479G>C (VPS13B)	XP_016868601.1:p.Met2493Ile
XM_024447074.1:c.10707G>C (VPS13B)	XP_024302842.1:p.Met3569Ile
NM_017890.5:c.11922G>C (VPS13B) MANE Plus Clinical	NP_060360.3:p.Met3974Ile
NM_152564.5:c.11847G>C (VPS13B) MANE Select	NP_689777.3:p.Met3949Ile