Canonical Allele Identifier: CA462341095

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100847963A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99835735A>T , CM000670.2:g.99835735A>T	GRCh38
NC_000008.10:g.100847963A>T , CM000670.1:g.100847963A>T	GRCh37
NC_000008.9:g.100917139A>T	NCBI36
NG_007098.2:g.827470A>T , LRG_351:g.827470A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.10014A>T	ENSP00000507923.1:p.Thr3338=
ENST00000682358.1:n.10084A>T
ENST00000683334.1:c.*5696A>T	ENSP00000507369.1:n.*5696A>T
ENST00000357162.7:c.9939A>T MANE Select	ENSP00000349685.2:p.Thr3313=
ENST00000358544.7:c.10014A>T MANE Plus Clinical	ENSP00000351346.2:p.Thr3338=
ENST00000357162.6:c.9939A>T	ENSP00000349685.2:p.Thr3313=
ENST00000358544.6:c.10014A>T	ENSP00000351346.2:p.Thr3338=
NM_017890.4:c.10014A>T , LRG_351t1:c.10014A>T	NP_060360.3:p.Thr3338=
NM_152564.4:c.9939A>T , LRG_351t2:c.9939A>T	NP_689777.3:p.Thr3313=
XM_005250800.2:c.10014A>T	XP_005250857.1:p.Thr3338=
XM_005250801.3:c.10014A>T	XP_005250858.1:p.Thr3338=
XM_011516848.1:c.10011A>T	XP_011515150.1:p.Thr3337=
XM_011516849.1:c.9936A>T	XP_011515151.1:p.Thr3312=
XM_011516850.1:c.9636A>T	XP_011515152.1:p.Thr3212=
XM_011516851.1:c.6900A>T	XP_011515153.1:p.Thr2300=
XM_011516852.1:c.6900A>T	XP_011515154.1:p.Thr2300=
XM_011516854.1:c.5793A>T	XP_011515156.1:p.Thr1931=
XM_005250800.3:c.10014A>T	XP_005250857.1:p.Thr3338=
XM_005250801.5:c.10014A>T	XP_005250858.1:p.Thr3338=
XM_011516848.2:c.10011A>T	XP_011515150.1:p.Thr3337=
XM_011516849.2:c.9936A>T	XP_011515151.1:p.Thr3312=
XM_011516850.2:c.9636A>T	XP_011515152.1:p.Thr3212=
XM_011516851.2:c.6900A>T	XP_011515153.1:p.Thr2300=
XM_011516852.2:c.6900A>T	XP_011515154.1:p.Thr2300=
XM_011516854.2:c.5793A>T	XP_011515156.1:p.Thr1931=
XM_017013109.1:c.9819A>T	XP_016868598.1:p.Thr3273=
XM_017013111.1:c.6900A>T	XP_016868600.1:p.Thr2300=
XM_017013112.1:c.5571A>T	XP_016868601.1:p.Thr1857=
XM_024447074.1:c.8799A>T	XP_024302842.1:p.Thr2933=
NM_017890.5:c.10014A>T MANE Plus Clinical	NP_060360.3:p.Thr3338=
NM_152564.5:c.9939A>T MANE Select	NP_689777.3:p.Thr3313=