Canonical Allele Identifier: CA371795863

Gene: VPS13B COX6C

Linked Data

• MyVariant Identifiers: chr8:g.100887779C>G (hg19) ; chr8:g.99875551C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99875551C>G , CM000670.2:g.99875551C>G	GRCh38
NC_000008.10:g.100887779C>G , CM000670.1:g.100887779C>G	GRCh37
NC_000008.9:g.100956955C>G	NCBI36
NG_007098.2:g.867286C>G , LRG_351:g.867286C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*1608C>G (VPS13B)	ENSP00000507923.1:n.*1608C>G
ENST00000682358.1:n.12584C>G (VPS13B)
ENST00000683334.1:c.*7636C>G (VPS13B)	ENSP00000507369.1:n.*7636C>G
ENST00000357162.7:c.11879C>G (VPS13B) MANE Select	ENSP00000349685.2:p.Pro3960Arg
ENST00000358544.7:c.11954C>G (VPS13B) MANE Plus Clinical	ENSP00000351346.2:p.Pro3985Arg
ENST00000357162.6:c.11879C>G (VPS13B)	ENSP00000349685.2:p.Pro3960Arg
ENST00000358544.6:c.11954C>G (VPS13B)	ENSP00000351346.2:p.Pro3985Arg
ENST00000493587.1:n.1456C>G (VPS13B)
ENST00000520517.5:c.*142-459G>C (COX6C)	ENSP00000429991.1:n.*142-459G>C
ENST00000522934.5:c.*142-2258G>C (COX6C)	ENSP00000428702.1:n.*142-2258G>C
NM_017890.4:c.11954C>G , LRG_351t1:c.11954C>G (VPS13B)	NP_060360.3:p.Pro3985Arg
NM_152564.4:c.11879C>G , LRG_351t2:c.11879C>G (VPS13B)	NP_689777.3:p.Pro3960Arg
XM_005250800.2:c.11954C>G (VPS13B)	XP_005250857.1:p.Pro3985Arg
XM_005250801.3:c.11954C>G (VPS13B)	XP_005250858.1:p.Pro3985Arg
XM_011516848.1:c.11951C>G (VPS13B)	XP_011515150.1:p.Pro3984Arg
XM_011516849.1:c.11876C>G (VPS13B)	XP_011515151.1:p.Pro3959Arg
XM_011516850.1:c.11576C>G (VPS13B)	XP_011515152.1:p.Pro3859Arg
XM_011516851.1:c.8840C>G (VPS13B)	XP_011515153.1:p.Pro2947Arg
XM_011516852.1:c.8840C>G (VPS13B)	XP_011515154.1:p.Pro2947Arg
XM_011516854.1:c.7733C>G (VPS13B)	XP_011515156.1:p.Pro2578Arg
XM_005250800.3:c.11954C>G (VPS13B)	XP_005250857.1:p.Pro3985Arg
XM_005250801.5:c.11954C>G (VPS13B)	XP_005250858.1:p.Pro3985Arg
XM_011516848.2:c.11951C>G (VPS13B)	XP_011515150.1:p.Pro3984Arg
XM_011516849.2:c.11876C>G (VPS13B)	XP_011515151.1:p.Pro3959Arg
XM_011516850.2:c.11576C>G (VPS13B)	XP_011515152.1:p.Pro3859Arg
XM_011516851.2:c.8840C>G (VPS13B)	XP_011515153.1:p.Pro2947Arg
XM_011516852.2:c.8840C>G (VPS13B)	XP_011515154.1:p.Pro2947Arg
XM_011516854.2:c.7733C>G (VPS13B)	XP_011515156.1:p.Pro2578Arg
XM_017013109.1:c.11759C>G (VPS13B)	XP_016868598.1:p.Pro3920Arg
XM_017013111.1:c.8840C>G (VPS13B)	XP_016868600.1:p.Pro2947Arg
XM_017013112.1:c.7511C>G (VPS13B)	XP_016868601.1:p.Pro2504Arg
XM_024447074.1:c.10739C>G (VPS13B)	XP_024302842.1:p.Pro3580Arg
NM_017890.5:c.11954C>G (VPS13B) MANE Plus Clinical	NP_060360.3:p.Pro3985Arg
NM_152564.5:c.11879C>G (VPS13B) MANE Select	NP_689777.3:p.Pro3960Arg