Canonical Allele Identifier: CA371865651

Gene: VPS13B

Linked Data

• COSMIC: COSM324252 ; COSM324253
• MyVariant Identifiers: chr8:g.100403825G>C (hg19) ; chr8:g.99391597G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99391597G>C , CM000670.2:g.99391597G>C	GRCh38
NC_000008.10:g.100403825G>C , CM000670.1:g.100403825G>C	GRCh37
NC_000008.9:g.100473001G>C	NCBI36
NG_007098.2:g.383332G>C , LRG_351:g.383332G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355155.6:c.2972G>C	ENSP00000347281.2:p.Arg991Thr
ENST00000682145.1:n.2852G>C
ENST00000682153.1:c.2975G>C	ENSP00000507923.1:p.Arg992Thr
ENST00000682234.1:c.2975G>C	ENSP00000508225.1:p.Arg992Thr
ENST00000682358.1:n.3045G>C
ENST00000683334.1:c.2975G>C	ENSP00000507369.1:p.Arg992Thr
ENST00000683486.1:n.3041G>C
ENST00000683619.1:n.3147G>C
ENST00000683869.1:n.3056G>C
ENST00000357162.7:c.2975G>C MANE Select	ENSP00000349685.2:p.Arg992Thr
ENST00000358544.7:c.2975G>C MANE Plus Clinical	ENSP00000351346.2:p.Arg992Thr
ENST00000357162.6:c.2975G>C	ENSP00000349685.2:p.Arg992Thr
ENST00000358544.6:c.2975G>C	ENSP00000351346.2:p.Arg992Thr
ENST00000496144.5:c.2975G>C	ENSP00000430900.1:p.Arg992Thr
ENST00000521037.1:n.146G>C
ENST00000522802.5:n.197G>C
NM_017890.4:c.2975G>C , LRG_351t1:c.2975G>C	NP_060360.3:p.Arg992Thr
NM_152564.4:c.2975G>C , LRG_351t2:c.2975G>C	NP_689777.3:p.Arg992Thr
XM_005250800.2:c.2975G>C	XP_005250857.1:p.Arg992Thr
XM_005250801.3:c.2975G>C	XP_005250858.1:p.Arg992Thr
XM_006716510.2:c.2975G>C	XP_006716573.1:p.Arg992Thr
XM_011516848.1:c.2972G>C	XP_011515150.1:p.Arg991Thr
XM_011516849.1:c.2975G>C	XP_011515151.1:p.Arg992Thr
XM_011516850.1:c.2597G>C	XP_011515152.1:p.Arg866Thr
XM_011516853.1:c.2975G>C	XP_011515155.1:p.Arg992Thr
XM_011516855.1:c.2975G>C	XP_011515157.1:p.Arg992Thr
XM_011516856.1:c.2975G>C	XP_011515158.1:p.Arg992Thr
XM_011516857.1:c.2975G>C	XP_011515159.1:p.Arg992Thr
XM_011516858.1:c.2975G>C	XP_011515160.1:p.Arg992Thr
XM_011516859.1:c.2975G>C	XP_011515161.1:p.Arg992Thr
XM_011516860.1:c.2975G>C	XP_011515162.1:p.Arg992Thr
XM_011516861.1:c.2975G>C	XP_011515163.1:p.Arg992Thr
XR_928301.1:n.3078G>C
XR_928302.1:n.3078G>C
XR_928303.1:n.3078G>C
XR_928304.1:n.3078G>C
XM_005250800.3:c.2975G>C	XP_005250857.1:p.Arg992Thr
XM_005250801.5:c.2975G>C	XP_005250858.1:p.Arg992Thr
XM_006716510.3:c.2975G>C	XP_006716573.1:p.Arg992Thr
XM_011516848.2:c.2972G>C	XP_011515150.1:p.Arg991Thr
XM_011516849.2:c.2975G>C	XP_011515151.1:p.Arg992Thr
XM_011516850.2:c.2597G>C	XP_011515152.1:p.Arg866Thr
XM_011516853.2:c.2975G>C	XP_011515155.1:p.Arg992Thr
XM_011516859.2:c.2975G>C	XP_011515161.1:p.Arg992Thr
XM_017013109.1:c.2780G>C	XP_016868598.1:p.Arg927Thr
XM_024447074.1:c.1760G>C	XP_024302842.1:p.Arg587Thr
XM_024447075.1:c.2975G>C	XP_024302843.1:p.Arg992Thr
XR_001745481.1:n.3078G>C
XR_001745482.2:n.3078G>C
XR_001745484.2:n.3078G>C
XR_002956601.1:n.3075G>C
XR_002956602.1:n.3078G>C
XR_928302.2:n.3078G>C
NM_017890.5:c.2975G>C MANE Plus Clinical	NP_060360.3:p.Arg992Thr
NM_152564.5:c.2975G>C MANE Select	NP_689777.3:p.Arg992Thr