Canonical Allele Identifier: CA183041712

Gene: VPS13B

Linked Data

• dbSNP Id: rs766832894
• MyVariant Identifiers: chr8:g.100789047T>C (hg19) ; chr8:g.99776819T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99776819T>C , CM000670.2:g.99776819T>C	GRCh38
NC_000008.10:g.100789047T>C , CM000670.1:g.100789047T>C	GRCh37
NC_000008.9:g.100858223T>C	NCBI36
NG_007098.2:g.768554T>C , LRG_351:g.768554T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.7367T>C	ENSP00000507923.1:p.Val2456Ala
ENST00000682358.1:n.7437T>C
ENST00000683334.1:c.*3049T>C	ENSP00000507369.1:n.*3049T>C
ENST00000357162.7:c.7292T>C MANE Select	ENSP00000349685.2:p.Val2431Ala
ENST00000358544.7:c.7367T>C MANE Plus Clinical	ENSP00000351346.2:p.Val2456Ala
ENST00000357162.6:c.7292T>C	ENSP00000349685.2:p.Val2431Ala
ENST00000358544.6:c.7367T>C	ENSP00000351346.2:p.Val2456Ala
ENST00000518569.1:n.378-1863T>C
NM_017890.4:c.7367T>C , LRG_351t1:c.7367T>C	NP_060360.3:p.Val2456Ala
NM_152564.4:c.7292T>C , LRG_351t2:c.7292T>C	NP_689777.3:p.Val2431Ala
XM_005250800.2:c.7367T>C	XP_005250857.1:p.Val2456Ala
XM_005250801.3:c.7367T>C	XP_005250858.1:p.Val2456Ala
XM_011516848.1:c.7364T>C	XP_011515150.1:p.Val2455Ala
XM_011516849.1:c.7289T>C	XP_011515151.1:p.Val2430Ala
XM_011516850.1:c.6989T>C	XP_011515152.1:p.Val2330Ala
XM_011516851.1:c.4253T>C	XP_011515153.1:p.Val1418Ala
XM_011516852.1:c.4253T>C	XP_011515154.1:p.Val1418Ala
XM_011516853.1:c.7367T>C	XP_011515155.1:p.Val2456Ala
XM_011516854.1:c.3146T>C	XP_011515156.1:p.Val1049Ala
XR_928446.1:n.1830+5659A>G
XM_005250800.3:c.7367T>C	XP_005250857.1:p.Val2456Ala
XM_005250801.5:c.7367T>C	XP_005250858.1:p.Val2456Ala
XM_011516848.2:c.7364T>C	XP_011515150.1:p.Val2455Ala
XM_011516849.2:c.7289T>C	XP_011515151.1:p.Val2430Ala
XM_011516850.2:c.6989T>C	XP_011515152.1:p.Val2330Ala
XM_011516851.2:c.4253T>C	XP_011515153.1:p.Val1418Ala
XM_011516852.2:c.4253T>C	XP_011515154.1:p.Val1418Ala
XM_011516853.2:c.7367T>C	XP_011515155.1:p.Val2456Ala
XM_011516854.2:c.3146T>C	XP_011515156.1:p.Val1049Ala
XM_017013109.1:c.7172T>C	XP_016868598.1:p.Val2391Ala
XM_017013111.1:c.4253T>C	XP_016868600.1:p.Val1418Ala
XM_017013112.1:c.2924T>C	XP_016868601.1:p.Val975Ala
XM_024447074.1:c.6152T>C	XP_024302842.1:p.Val2051Ala
NM_017890.5:c.7367T>C MANE Plus Clinical	NP_060360.3:p.Val2456Ala
NM_152564.5:c.7292T>C MANE Select	NP_689777.3:p.Val2431Ala