Canonical Allele Identifier: CA371874064

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100711809C>G (hg19) ; chr8:g.99699581C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99699581C>G , CM000670.2:g.99699581C>G	GRCh38
NC_000008.10:g.100711809C>G , CM000670.1:g.100711809C>G	GRCh37
NC_000008.9:g.100780985C>G	NCBI36
NG_007098.2:g.691316C>G , LRG_351:g.691316C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.6178C>G	ENSP00000507923.1:p.Leu2060Val
ENST00000682358.1:n.6248C>G
ENST00000683334.1:c.*1860C>G	ENSP00000507369.1:n.*1860C>G
ENST00000357162.7:c.6103C>G MANE Select	ENSP00000349685.2:p.Leu2035Val
ENST00000358544.7:c.6178C>G MANE Plus Clinical	ENSP00000351346.2:p.Leu2060Val
ENST00000357162.6:c.6103C>G	ENSP00000349685.2:p.Leu2035Val
ENST00000358544.6:c.6178C>G	ENSP00000351346.2:p.Leu2060Val
NM_017890.4:c.6178C>G , LRG_351t1:c.6178C>G	NP_060360.3:p.Leu2060Val
NM_152564.4:c.6103C>G , LRG_351t2:c.6103C>G	NP_689777.3:p.Leu2035Val
XM_005250800.2:c.6178C>G	XP_005250857.1:p.Leu2060Val
XM_005250801.3:c.6178C>G	XP_005250858.1:p.Leu2060Val
XM_011516848.1:c.6175C>G	XP_011515150.1:p.Leu2059Val
XM_011516849.1:c.6100C>G	XP_011515151.1:p.Leu2034Val
XM_011516850.1:c.5800C>G	XP_011515152.1:p.Leu1934Val
XM_011516851.1:c.3064C>G	XP_011515153.1:p.Leu1022Val
XM_011516852.1:c.3064C>G	XP_011515154.1:p.Leu1022Val
XM_011516853.1:c.6178C>G	XP_011515155.1:p.Leu2060Val
XM_011516854.1:c.1957C>G	XP_011515156.1:p.Leu653Val
XM_005250800.3:c.6178C>G	XP_005250857.1:p.Leu2060Val
XM_005250801.5:c.6178C>G	XP_005250858.1:p.Leu2060Val
XM_011516848.2:c.6175C>G	XP_011515150.1:p.Leu2059Val
XM_011516849.2:c.6100C>G	XP_011515151.1:p.Leu2034Val
XM_011516850.2:c.5800C>G	XP_011515152.1:p.Leu1934Val
XM_011516851.2:c.3064C>G	XP_011515153.1:p.Leu1022Val
XM_011516852.2:c.3064C>G	XP_011515154.1:p.Leu1022Val
XM_011516853.2:c.6178C>G	XP_011515155.1:p.Leu2060Val
XM_011516854.2:c.1957C>G	XP_011515156.1:p.Leu653Val
XM_017013109.1:c.5983C>G	XP_016868598.1:p.Leu1995Val
XM_017013111.1:c.3064C>G	XP_016868600.1:p.Leu1022Val
XM_017013112.1:c.1735C>G	XP_016868601.1:p.Leu579Val
XM_024447074.1:c.4963C>G	XP_024302842.1:p.Leu1655Val
NM_017890.5:c.6178C>G MANE Plus Clinical	NP_060360.3:p.Leu2060Val
NM_152564.5:c.6103C>G MANE Select	NP_689777.3:p.Leu2035Val