Canonical Allele Identifier: CA371795754

Gene: VPS13B COX6C

Linked Data

• MyVariant Identifiers: chr8:g.100887752T>A (hg19) ; chr8:g.99875524T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99875524T>A , CM000670.2:g.99875524T>A	GRCh38
NC_000008.10:g.100887752T>A , CM000670.1:g.100887752T>A	GRCh37
NC_000008.9:g.100956928T>A	NCBI36
NG_007098.2:g.867259T>A , LRG_351:g.867259T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*1581T>A (VPS13B)	ENSP00000507923.1:n.*1581T>A
ENST00000682358.1:n.12557T>A (VPS13B)
ENST00000683334.1:c.*7609T>A (VPS13B)	ENSP00000507369.1:n.*7609T>A
ENST00000357162.7:c.11852T>A (VPS13B) MANE Select	ENSP00000349685.2:p.Ile3951Lys
ENST00000358544.7:c.11927T>A (VPS13B) MANE Plus Clinical	ENSP00000351346.2:p.Ile3976Lys
ENST00000357162.6:c.11852T>A (VPS13B)	ENSP00000349685.2:p.Ile3951Lys
ENST00000358544.6:c.11927T>A (VPS13B)	ENSP00000351346.2:p.Ile3976Lys
ENST00000493587.1:n.1429T>A (VPS13B)
ENST00000520517.5:c.*142-432A>T (COX6C)	ENSP00000429991.1:n.*142-432A>T
ENST00000522934.5:c.*142-2231A>T (COX6C)	ENSP00000428702.1:n.*142-2231A>T
NM_017890.4:c.11927T>A , LRG_351t1:c.11927T>A (VPS13B)	NP_060360.3:p.Ile3976Lys
NM_152564.4:c.11852T>A , LRG_351t2:c.11852T>A (VPS13B)	NP_689777.3:p.Ile3951Lys
XM_005250800.2:c.11927T>A (VPS13B)	XP_005250857.1:p.Ile3976Lys
XM_005250801.3:c.11927T>A (VPS13B)	XP_005250858.1:p.Ile3976Lys
XM_011516848.1:c.11924T>A (VPS13B)	XP_011515150.1:p.Ile3975Lys
XM_011516849.1:c.11849T>A (VPS13B)	XP_011515151.1:p.Ile3950Lys
XM_011516850.1:c.11549T>A (VPS13B)	XP_011515152.1:p.Ile3850Lys
XM_011516851.1:c.8813T>A (VPS13B)	XP_011515153.1:p.Ile2938Lys
XM_011516852.1:c.8813T>A (VPS13B)	XP_011515154.1:p.Ile2938Lys
XM_011516854.1:c.7706T>A (VPS13B)	XP_011515156.1:p.Ile2569Lys
XM_005250800.3:c.11927T>A (VPS13B)	XP_005250857.1:p.Ile3976Lys
XM_005250801.5:c.11927T>A (VPS13B)	XP_005250858.1:p.Ile3976Lys
XM_011516848.2:c.11924T>A (VPS13B)	XP_011515150.1:p.Ile3975Lys
XM_011516849.2:c.11849T>A (VPS13B)	XP_011515151.1:p.Ile3950Lys
XM_011516850.2:c.11549T>A (VPS13B)	XP_011515152.1:p.Ile3850Lys
XM_011516851.2:c.8813T>A (VPS13B)	XP_011515153.1:p.Ile2938Lys
XM_011516852.2:c.8813T>A (VPS13B)	XP_011515154.1:p.Ile2938Lys
XM_011516854.2:c.7706T>A (VPS13B)	XP_011515156.1:p.Ile2569Lys
XM_017013109.1:c.11732T>A (VPS13B)	XP_016868598.1:p.Ile3911Lys
XM_017013111.1:c.8813T>A (VPS13B)	XP_016868600.1:p.Ile2938Lys
XM_017013112.1:c.7484T>A (VPS13B)	XP_016868601.1:p.Ile2495Lys
XM_024447074.1:c.10712T>A (VPS13B)	XP_024302842.1:p.Ile3571Lys
NM_017890.5:c.11927T>A (VPS13B) MANE Plus Clinical	NP_060360.3:p.Ile3976Lys
NM_152564.5:c.11852T>A (VPS13B) MANE Select	NP_689777.3:p.Ile3951Lys