Canonical Allele Identifier: CA371872526

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100654245T>G (hg19) ; chr8:g.99642017T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99642017T>G , CM000670.2:g.99642017T>G	GRCh38
NC_000008.10:g.100654245T>G , CM000670.1:g.100654245T>G	GRCh37
NC_000008.9:g.100723421T>G	NCBI36
NG_007098.2:g.633752T>G , LRG_351:g.633752T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.5502T>G	ENSP00000507923.1:p.Phe1834Leu
ENST00000682358.1:n.5572T>G
ENST00000683334.1:c.*1184T>G	ENSP00000507369.1:n.*1184T>G
ENST00000357162.7:c.5427T>G MANE Select	ENSP00000349685.2:p.Phe1809Leu
ENST00000358544.7:c.5502T>G MANE Plus Clinical	ENSP00000351346.2:p.Phe1834Leu
ENST00000357162.6:c.5427T>G	ENSP00000349685.2:p.Phe1809Leu
ENST00000358544.6:c.5502T>G	ENSP00000351346.2:p.Phe1834Leu
NM_017890.4:c.5502T>G , LRG_351t1:c.5502T>G	NP_060360.3:p.Phe1834Leu
NM_152564.4:c.5427T>G , LRG_351t2:c.5427T>G	NP_689777.3:p.Phe1809Leu
XM_005250800.2:c.5502T>G	XP_005250857.1:p.Phe1834Leu
XM_005250801.3:c.5502T>G	XP_005250858.1:p.Phe1834Leu
XM_011516848.1:c.5499T>G	XP_011515150.1:p.Phe1833Leu
XM_011516849.1:c.5424T>G	XP_011515151.1:p.Phe1808Leu
XM_011516850.1:c.5124T>G	XP_011515152.1:p.Phe1708Leu
XM_011516851.1:c.2388T>G	XP_011515153.1:p.Phe796Leu
XM_011516852.1:c.2388T>G	XP_011515154.1:p.Phe796Leu
XM_011516853.1:c.5502T>G	XP_011515155.1:p.Phe1834Leu
XM_011516854.1:c.1281T>G	XP_011515156.1:p.Phe427Leu
XM_005250800.3:c.5502T>G	XP_005250857.1:p.Phe1834Leu
XM_005250801.5:c.5502T>G	XP_005250858.1:p.Phe1834Leu
XM_011516848.2:c.5499T>G	XP_011515150.1:p.Phe1833Leu
XM_011516849.2:c.5424T>G	XP_011515151.1:p.Phe1808Leu
XM_011516850.2:c.5124T>G	XP_011515152.1:p.Phe1708Leu
XM_011516851.2:c.2388T>G	XP_011515153.1:p.Phe796Leu
XM_011516852.2:c.2388T>G	XP_011515154.1:p.Phe796Leu
XM_011516853.2:c.5502T>G	XP_011515155.1:p.Phe1834Leu
XM_011516854.2:c.1281T>G	XP_011515156.1:p.Phe427Leu
XM_017013109.1:c.5307T>G	XP_016868598.1:p.Phe1769Leu
XM_017013111.1:c.2388T>G	XP_016868600.1:p.Phe796Leu
XM_017013112.1:c.1059T>G	XP_016868601.1:p.Phe353Leu
XM_024447074.1:c.4287T>G	XP_024302842.1:p.Phe1429Leu
XR_001745482.2:n.5463T>G
NM_017890.5:c.5502T>G MANE Plus Clinical	NP_060360.3:p.Phe1834Leu
NM_152564.5:c.5427T>G MANE Select	NP_689777.3:p.Phe1809Leu