Canonical Allele Identifier: CA462458477

Gene: VPS13B COX6C

Linked Data

• MyVariant Identifiers: chr8:g.100887753A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99875525A>C , CM000670.2:g.99875525A>C	GRCh38
NC_000008.10:g.100887753A>C , CM000670.1:g.100887753A>C	GRCh37
NC_000008.9:g.100956929A>C	NCBI36
NG_007098.2:g.867260A>C , LRG_351:g.867260A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*1582A>C (VPS13B)	ENSP00000507923.1:n.*1582A>C
ENST00000682358.1:n.12558A>C (VPS13B)
ENST00000683334.1:c.*7610A>C (VPS13B)	ENSP00000507369.1:n.*7610A>C
ENST00000357162.7:c.11853A>C (VPS13B) MANE Select	ENSP00000349685.2:p.Ile3951=
ENST00000358544.7:c.11928A>C (VPS13B) MANE Plus Clinical	ENSP00000351346.2:p.Ile3976=
ENST00000357162.6:c.11853A>C (VPS13B)	ENSP00000349685.2:p.Ile3951=
ENST00000358544.6:c.11928A>C (VPS13B)	ENSP00000351346.2:p.Ile3976=
ENST00000493587.1:n.1430A>C (VPS13B)
ENST00000520517.5:c.*142-433T>G (COX6C)	ENSP00000429991.1:n.*142-433T>G
ENST00000522934.5:c.*142-2232T>G (COX6C)	ENSP00000428702.1:n.*142-2232T>G
NM_017890.4:c.11928A>C , LRG_351t1:c.11928A>C (VPS13B)	NP_060360.3:p.Ile3976=
NM_152564.4:c.11853A>C , LRG_351t2:c.11853A>C (VPS13B)	NP_689777.3:p.Ile3951=
XM_005250800.2:c.11928A>C (VPS13B)	XP_005250857.1:p.Ile3976=
XM_005250801.3:c.11928A>C (VPS13B)	XP_005250858.1:p.Ile3976=
XM_011516848.1:c.11925A>C (VPS13B)	XP_011515150.1:p.Ile3975=
XM_011516849.1:c.11850A>C (VPS13B)	XP_011515151.1:p.Ile3950=
XM_011516850.1:c.11550A>C (VPS13B)	XP_011515152.1:p.Ile3850=
XM_011516851.1:c.8814A>C (VPS13B)	XP_011515153.1:p.Ile2938=
XM_011516852.1:c.8814A>C (VPS13B)	XP_011515154.1:p.Ile2938=
XM_011516854.1:c.7707A>C (VPS13B)	XP_011515156.1:p.Ile2569=
XM_005250800.3:c.11928A>C (VPS13B)	XP_005250857.1:p.Ile3976=
XM_005250801.5:c.11928A>C (VPS13B)	XP_005250858.1:p.Ile3976=
XM_011516848.2:c.11925A>C (VPS13B)	XP_011515150.1:p.Ile3975=
XM_011516849.2:c.11850A>C (VPS13B)	XP_011515151.1:p.Ile3950=
XM_011516850.2:c.11550A>C (VPS13B)	XP_011515152.1:p.Ile3850=
XM_011516851.2:c.8814A>C (VPS13B)	XP_011515153.1:p.Ile2938=
XM_011516852.2:c.8814A>C (VPS13B)	XP_011515154.1:p.Ile2938=
XM_011516854.2:c.7707A>C (VPS13B)	XP_011515156.1:p.Ile2569=
XM_017013109.1:c.11733A>C (VPS13B)	XP_016868598.1:p.Ile3911=
XM_017013111.1:c.8814A>C (VPS13B)	XP_016868600.1:p.Ile2938=
XM_017013112.1:c.7485A>C (VPS13B)	XP_016868601.1:p.Ile2495=
XM_024447074.1:c.10713A>C (VPS13B)	XP_024302842.1:p.Ile3571=
NM_017890.5:c.11928A>C (VPS13B) MANE Plus Clinical	NP_060360.3:p.Ile3976=
NM_152564.5:c.11853A>C (VPS13B) MANE Select	NP_689777.3:p.Ile3951=