Canonical Allele Identifier: CA371875846

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100789150C>G (hg19) ; chr8:g.99776922C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99776922C>G , CM000670.2:g.99776922C>G	GRCh38
NC_000008.10:g.100789150C>G , CM000670.1:g.100789150C>G	GRCh37
NC_000008.9:g.100858326C>G	NCBI36
NG_007098.2:g.768657C>G , LRG_351:g.768657C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.7470C>G	ENSP00000507923.1:p.Phe2490Leu
ENST00000682358.1:n.7540C>G
ENST00000683334.1:c.*3152C>G	ENSP00000507369.1:n.*3152C>G
ENST00000357162.7:c.7395C>G MANE Select	ENSP00000349685.2:p.Phe2465Leu
ENST00000358544.7:c.7470C>G MANE Plus Clinical	ENSP00000351346.2:p.Phe2490Leu
ENST00000357162.6:c.7395C>G	ENSP00000349685.2:p.Phe2465Leu
ENST00000358544.6:c.7470C>G	ENSP00000351346.2:p.Phe2490Leu
ENST00000518569.1:n.378-1760C>G
NM_017890.4:c.7470C>G , LRG_351t1:c.7470C>G	NP_060360.3:p.Phe2490Leu
NM_152564.4:c.7395C>G , LRG_351t2:c.7395C>G	NP_689777.3:p.Phe2465Leu
XM_005250800.2:c.7470C>G	XP_005250857.1:p.Phe2490Leu
XM_005250801.3:c.7470C>G	XP_005250858.1:p.Phe2490Leu
XM_011516848.1:c.7467C>G	XP_011515150.1:p.Phe2489Leu
XM_011516849.1:c.7392C>G	XP_011515151.1:p.Phe2464Leu
XM_011516850.1:c.7092C>G	XP_011515152.1:p.Phe2364Leu
XM_011516851.1:c.4356C>G	XP_011515153.1:p.Phe1452Leu
XM_011516852.1:c.4356C>G	XP_011515154.1:p.Phe1452Leu
XM_011516853.1:c.7470C>G	XP_011515155.1:p.Phe2490Leu
XM_011516854.1:c.3249C>G	XP_011515156.1:p.Phe1083Leu
XR_928446.1:n.1830+5556G>C
XM_005250800.3:c.7470C>G	XP_005250857.1:p.Phe2490Leu
XM_005250801.5:c.7470C>G	XP_005250858.1:p.Phe2490Leu
XM_011516848.2:c.7467C>G	XP_011515150.1:p.Phe2489Leu
XM_011516849.2:c.7392C>G	XP_011515151.1:p.Phe2464Leu
XM_011516850.2:c.7092C>G	XP_011515152.1:p.Phe2364Leu
XM_011516851.2:c.4356C>G	XP_011515153.1:p.Phe1452Leu
XM_011516852.2:c.4356C>G	XP_011515154.1:p.Phe1452Leu
XM_011516853.2:c.7470C>G	XP_011515155.1:p.Phe2490Leu
XM_011516854.2:c.3249C>G	XP_011515156.1:p.Phe1083Leu
XM_017013109.1:c.7275C>G	XP_016868598.1:p.Phe2425Leu
XM_017013111.1:c.4356C>G	XP_016868600.1:p.Phe1452Leu
XM_017013112.1:c.3027C>G	XP_016868601.1:p.Phe1009Leu
XM_024447074.1:c.6255C>G	XP_024302842.1:p.Phe2085Leu
NM_017890.5:c.7470C>G MANE Plus Clinical	NP_060360.3:p.Phe2490Leu
NM_152564.5:c.7395C>G MANE Select	NP_689777.3:p.Phe2465Leu