Canonical Allele Identifier: CA371795910

Gene: VPS13B COX6C

Linked Data

• dbSNP Id: rs1167108439
• gnomAD v3: 8-99875565-G-T
• gnomAD v4: 8-99875565-G-T
• MyVariant Identifiers: chr8:g.100887793G>T (hg19) ; chr8:g.99875565G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99875565G>T , CM000670.2:g.99875565G>T	GRCh38
NC_000008.10:g.100887793G>T , CM000670.1:g.100887793G>T	GRCh37
NC_000008.9:g.100956969G>T	NCBI36
NG_007098.2:g.867300G>T , LRG_351:g.867300G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682153.1:c.*1622G>T (VPS13B)	ENSP00000507923.1:n.*1622G>T
ENST00000682358.1:n.12598G>T (VPS13B)
ENST00000683334.1:c.*7650G>T (VPS13B)	ENSP00000507369.1:n.*7650G>T
ENST00000357162.7:c.11893G>T (VPS13B) MANE Select	ENSP00000349685.2:p.Val3965Phe
ENST00000358544.7:c.11968G>T (VPS13B) MANE Plus Clinical	ENSP00000351346.2:p.Val3990Phe
ENST00000357162.6:c.11893G>T (VPS13B)	ENSP00000349685.2:p.Val3965Phe
ENST00000358544.6:c.11968G>T (VPS13B)	ENSP00000351346.2:p.Val3990Phe
ENST00000493587.1:n.1470G>T (VPS13B)
ENST00000520517.5:c.*142-473C>A (COX6C)	ENSP00000429991.1:n.*142-473C>A
ENST00000522934.5:c.*142-2272C>A (COX6C)	ENSP00000428702.1:n.*142-2272C>A
NM_017890.4:c.11968G>T , LRG_351t1:c.11968G>T (VPS13B)	NP_060360.3:p.Val3990Phe
NM_152564.4:c.11893G>T , LRG_351t2:c.11893G>T (VPS13B)	NP_689777.3:p.Val3965Phe
XM_005250800.2:c.11968G>T (VPS13B)	XP_005250857.1:p.Val3990Phe
XM_005250801.3:c.11968G>T (VPS13B)	XP_005250858.1:p.Val3990Phe
XM_011516848.1:c.11965G>T (VPS13B)	XP_011515150.1:p.Val3989Phe
XM_011516849.1:c.11890G>T (VPS13B)	XP_011515151.1:p.Val3964Phe
XM_011516850.1:c.11590G>T (VPS13B)	XP_011515152.1:p.Val3864Phe
XM_011516851.1:c.8854G>T (VPS13B)	XP_011515153.1:p.Val2952Phe
XM_011516852.1:c.8854G>T (VPS13B)	XP_011515154.1:p.Val2952Phe
XM_011516854.1:c.7747G>T (VPS13B)	XP_011515156.1:p.Val2583Phe
XM_005250800.3:c.11968G>T (VPS13B)	XP_005250857.1:p.Val3990Phe
XM_005250801.5:c.11968G>T (VPS13B)	XP_005250858.1:p.Val3990Phe
XM_011516848.2:c.11965G>T (VPS13B)	XP_011515150.1:p.Val3989Phe
XM_011516849.2:c.11890G>T (VPS13B)	XP_011515151.1:p.Val3964Phe
XM_011516850.2:c.11590G>T (VPS13B)	XP_011515152.1:p.Val3864Phe
XM_011516851.2:c.8854G>T (VPS13B)	XP_011515153.1:p.Val2952Phe
XM_011516852.2:c.8854G>T (VPS13B)	XP_011515154.1:p.Val2952Phe
XM_011516854.2:c.7747G>T (VPS13B)	XP_011515156.1:p.Val2583Phe
XM_017013109.1:c.11773G>T (VPS13B)	XP_016868598.1:p.Val3925Phe
XM_017013111.1:c.8854G>T (VPS13B)	XP_016868600.1:p.Val2952Phe
XM_017013112.1:c.7525G>T (VPS13B)	XP_016868601.1:p.Val2509Phe
XM_024447074.1:c.10753G>T (VPS13B)	XP_024302842.1:p.Val3585Phe
NM_017890.5:c.11968G>T (VPS13B) MANE Plus Clinical	NP_060360.3:p.Val3990Phe
NM_152564.5:c.11893G>T (VPS13B) MANE Select	NP_689777.3:p.Val3965Phe