Canonical Allele Identifier: CA462458577

Gene: VPS13B COX6C

Linked Data

• MyVariant Identifiers: chr8:g.100887696G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99875468G>C , CM000670.2:g.99875468G>C	GRCh38
NC_000008.10:g.100887696G>C , CM000670.1:g.100887696G>C	GRCh37
NC_000008.9:g.100956872G>C	NCBI36
NG_007098.2:g.867203G>C , LRG_351:g.867203G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*1525G>C (VPS13B)	ENSP00000507923.1:n.*1525G>C
ENST00000682358.1:n.12501G>C (VPS13B)
ENST00000683334.1:c.*7553G>C (VPS13B)	ENSP00000507369.1:n.*7553G>C
ENST00000357162.7:c.11796G>C (VPS13B) MANE Select	ENSP00000349685.2:p.Val3932=
ENST00000358544.7:c.11871G>C (VPS13B) MANE Plus Clinical	ENSP00000351346.2:p.Val3957=
ENST00000357162.6:c.11796G>C (VPS13B)	ENSP00000349685.2:p.Val3932=
ENST00000358544.6:c.11871G>C (VPS13B)	ENSP00000351346.2:p.Val3957=
ENST00000493587.1:n.1373G>C (VPS13B)
ENST00000520517.5:c.*142-376C>G (COX6C)	ENSP00000429991.1:n.*142-376C>G
ENST00000522934.5:c.*142-2175C>G (COX6C)	ENSP00000428702.1:n.*142-2175C>G
NM_017890.4:c.11871G>C , LRG_351t1:c.11871G>C (VPS13B)	NP_060360.3:p.Val3957=
NM_152564.4:c.11796G>C , LRG_351t2:c.11796G>C (VPS13B)	NP_689777.3:p.Val3932=
XM_005250800.2:c.11871G>C (VPS13B)	XP_005250857.1:p.Val3957=
XM_005250801.3:c.11871G>C (VPS13B)	XP_005250858.1:p.Val3957=
XM_011516848.1:c.11868G>C (VPS13B)	XP_011515150.1:p.Val3956=
XM_011516849.1:c.11793G>C (VPS13B)	XP_011515151.1:p.Val3931=
XM_011516850.1:c.11493G>C (VPS13B)	XP_011515152.1:p.Val3831=
XM_011516851.1:c.8757G>C (VPS13B)	XP_011515153.1:p.Val2919=
XM_011516852.1:c.8757G>C (VPS13B)	XP_011515154.1:p.Val2919=
XM_011516854.1:c.7650G>C (VPS13B)	XP_011515156.1:p.Val2550=
XM_005250800.3:c.11871G>C (VPS13B)	XP_005250857.1:p.Val3957=
XM_005250801.5:c.11871G>C (VPS13B)	XP_005250858.1:p.Val3957=
XM_011516848.2:c.11868G>C (VPS13B)	XP_011515150.1:p.Val3956=
XM_011516849.2:c.11793G>C (VPS13B)	XP_011515151.1:p.Val3931=
XM_011516850.2:c.11493G>C (VPS13B)	XP_011515152.1:p.Val3831=
XM_011516851.2:c.8757G>C (VPS13B)	XP_011515153.1:p.Val2919=
XM_011516852.2:c.8757G>C (VPS13B)	XP_011515154.1:p.Val2919=
XM_011516854.2:c.7650G>C (VPS13B)	XP_011515156.1:p.Val2550=
XM_017013109.1:c.11676G>C (VPS13B)	XP_016868598.1:p.Val3892=
XM_017013111.1:c.8757G>C (VPS13B)	XP_016868600.1:p.Val2919=
XM_017013112.1:c.7428G>C (VPS13B)	XP_016868601.1:p.Val2476=
XM_024447074.1:c.10656G>C (VPS13B)	XP_024302842.1:p.Val3552=
NM_017890.5:c.11871G>C (VPS13B) MANE Plus Clinical	NP_060360.3:p.Val3957=
NM_152564.5:c.11796G>C (VPS13B) MANE Select	NP_689777.3:p.Val3932=