Canonical Allele Identifier: CA371795918

Gene: VPS13B COX6C

Linked Data

• MyVariant Identifiers: chr8:g.100887794T>A (hg19) ; chr8:g.99875566T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99875566T>A , CM000670.2:g.99875566T>A	GRCh38
NC_000008.10:g.100887794T>A , CM000670.1:g.100887794T>A	GRCh37
NC_000008.9:g.100956970T>A	NCBI36
NG_007098.2:g.867301T>A , LRG_351:g.867301T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*1623T>A (VPS13B)	ENSP00000507923.1:n.*1623T>A
ENST00000682358.1:n.12599T>A (VPS13B)
ENST00000683334.1:c.*7651T>A (VPS13B)	ENSP00000507369.1:n.*7651T>A
ENST00000357162.7:c.11894T>A (VPS13B) MANE Select	ENSP00000349685.2:p.Val3965Asp
ENST00000358544.7:c.11969T>A (VPS13B) MANE Plus Clinical	ENSP00000351346.2:p.Val3990Asp
ENST00000357162.6:c.11894T>A (VPS13B)	ENSP00000349685.2:p.Val3965Asp
ENST00000358544.6:c.11969T>A (VPS13B)	ENSP00000351346.2:p.Val3990Asp
ENST00000493587.1:n.1471T>A (VPS13B)
ENST00000520517.5:c.*142-474A>T (COX6C)	ENSP00000429991.1:n.*142-474A>T
ENST00000522934.5:c.*142-2273A>T (COX6C)	ENSP00000428702.1:n.*142-2273A>T
NM_017890.4:c.11969T>A , LRG_351t1:c.11969T>A (VPS13B)	NP_060360.3:p.Val3990Asp
NM_152564.4:c.11894T>A , LRG_351t2:c.11894T>A (VPS13B)	NP_689777.3:p.Val3965Asp
XM_005250800.2:c.11969T>A (VPS13B)	XP_005250857.1:p.Val3990Asp
XM_005250801.3:c.11969T>A (VPS13B)	XP_005250858.1:p.Val3990Asp
XM_011516848.1:c.11966T>A (VPS13B)	XP_011515150.1:p.Val3989Asp
XM_011516849.1:c.11891T>A (VPS13B)	XP_011515151.1:p.Val3964Asp
XM_011516850.1:c.11591T>A (VPS13B)	XP_011515152.1:p.Val3864Asp
XM_011516851.1:c.8855T>A (VPS13B)	XP_011515153.1:p.Val2952Asp
XM_011516852.1:c.8855T>A (VPS13B)	XP_011515154.1:p.Val2952Asp
XM_011516854.1:c.7748T>A (VPS13B)	XP_011515156.1:p.Val2583Asp
XM_005250800.3:c.11969T>A (VPS13B)	XP_005250857.1:p.Val3990Asp
XM_005250801.5:c.11969T>A (VPS13B)	XP_005250858.1:p.Val3990Asp
XM_011516848.2:c.11966T>A (VPS13B)	XP_011515150.1:p.Val3989Asp
XM_011516849.2:c.11891T>A (VPS13B)	XP_011515151.1:p.Val3964Asp
XM_011516850.2:c.11591T>A (VPS13B)	XP_011515152.1:p.Val3864Asp
XM_011516851.2:c.8855T>A (VPS13B)	XP_011515153.1:p.Val2952Asp
XM_011516852.2:c.8855T>A (VPS13B)	XP_011515154.1:p.Val2952Asp
XM_011516854.2:c.7748T>A (VPS13B)	XP_011515156.1:p.Val2583Asp
XM_017013109.1:c.11774T>A (VPS13B)	XP_016868598.1:p.Val3925Asp
XM_017013111.1:c.8855T>A (VPS13B)	XP_016868600.1:p.Val2952Asp
XM_017013112.1:c.7526T>A (VPS13B)	XP_016868601.1:p.Val2509Asp
XM_024447074.1:c.10754T>A (VPS13B)	XP_024302842.1:p.Val3585Asp
NM_017890.5:c.11969T>A (VPS13B) MANE Plus Clinical	NP_060360.3:p.Val3990Asp
NM_152564.5:c.11894T>A (VPS13B) MANE Select	NP_689777.3:p.Val3965Asp