Canonical Allele Identifier: CA371793715

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100883096A>T (hg19) ; chr8:g.99870868A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99870868A>T , CM000670.2:g.99870868A>T	GRCh38
NC_000008.10:g.100883096A>T , CM000670.1:g.100883096A>T	GRCh37
NC_000008.9:g.100952272A>T	NCBI36
NG_007098.2:g.862603A>T , LRG_351:g.862603A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682153.1:c.*645A>T	ENSP00000507923.1:n.*645A>T
ENST00000682358.1:n.11621A>T
ENST00000683334.1:c.*7233A>T	ENSP00000507369.1:n.*7233A>T
ENST00000357162.7:c.11476A>T MANE Select	ENSP00000349685.2:p.Ser3826Cys
ENST00000358544.7:c.11551A>T MANE Plus Clinical	ENSP00000351346.2:p.Ser3851Cys
ENST00000357162.6:c.11476A>T	ENSP00000349685.2:p.Ser3826Cys
ENST00000358544.6:c.11551A>T	ENSP00000351346.2:p.Ser3851Cys
ENST00000493587.1:n.493A>T
NM_017890.4:c.11551A>T , LRG_351t1:c.11551A>T	NP_060360.3:p.Ser3851Cys
NM_152564.4:c.11476A>T , LRG_351t2:c.11476A>T	NP_689777.3:p.Ser3826Cys
XM_005250800.2:c.11551A>T	XP_005250857.1:p.Ser3851Cys
XM_005250801.3:c.11551A>T	XP_005250858.1:p.Ser3851Cys
XM_011516848.1:c.11548A>T	XP_011515150.1:p.Ser3850Cys
XM_011516849.1:c.11473A>T	XP_011515151.1:p.Ser3825Cys
XM_011516850.1:c.11173A>T	XP_011515152.1:p.Ser3725Cys
XM_011516851.1:c.8437A>T	XP_011515153.1:p.Ser2813Cys
XM_011516852.1:c.8437A>T	XP_011515154.1:p.Ser2813Cys
XM_011516854.1:c.7330A>T	XP_011515156.1:p.Ser2444Cys
XM_005250800.3:c.11551A>T	XP_005250857.1:p.Ser3851Cys
XM_005250801.5:c.11551A>T	XP_005250858.1:p.Ser3851Cys
XM_011516848.2:c.11548A>T	XP_011515150.1:p.Ser3850Cys
XM_011516849.2:c.11473A>T	XP_011515151.1:p.Ser3825Cys
XM_011516850.2:c.11173A>T	XP_011515152.1:p.Ser3725Cys
XM_011516851.2:c.8437A>T	XP_011515153.1:p.Ser2813Cys
XM_011516852.2:c.8437A>T	XP_011515154.1:p.Ser2813Cys
XM_011516854.2:c.7330A>T	XP_011515156.1:p.Ser2444Cys
XM_017013109.1:c.11356A>T	XP_016868598.1:p.Ser3786Cys
XM_017013111.1:c.8437A>T	XP_016868600.1:p.Ser2813Cys
XM_017013112.1:c.7108A>T	XP_016868601.1:p.Ser2370Cys
XM_024447074.1:c.10336A>T	XP_024302842.1:p.Ser3446Cys
NM_017890.5:c.11551A>T MANE Plus Clinical	NP_060360.3:p.Ser3851Cys
NM_152564.5:c.11476A>T MANE Select	NP_689777.3:p.Ser3826Cys