Canonical Allele Identifier: CA1805821085
Gene: VPS13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.99642062G= , CM000670.2:g.99642062G= GRCh38
NC_000008.10:g.100654290G= , CM000670.1:g.100654290G= GRCh37
NC_000008.9:g.100723466G= NCBI36
NG_007098.2:g.633797G= , LRG_351:g.633797G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682153.1:c.5547G= ENSP00000507923.1:p.Met1849=
ENST00000682358.1:n.5617G=
ENST00000683334.1:c.*1229G= ENSP00000507369.1:n.*1229G=
ENST00000357162.7:c.5472G= MANE Select ENSP00000349685.2:p.Met1824=
ENST00000358544.7:c.5547G= MANE Plus Clinical ENSP00000351346.2:p.Met1849=
ENST00000357162.6:c.5472G= ENSP00000349685.2:p.Met1824=
ENST00000358544.6:c.5547G= ENSP00000351346.2:p.Met1849=
NM_017890.4:c.5547G= , LRG_351t1:c.5547G= NP_060360.3:p.Met1849=
NM_152564.4:c.5472G= , LRG_351t2:c.5472G= NP_689777.3:p.Met1824=
XM_005250800.2:c.5547G= XP_005250857.1:p.Met1849=
XM_005250801.3:c.5547G= XP_005250858.1:p.Met1849=
XM_011516848.1:c.5544G= XP_011515150.1:p.Met1848=
XM_011516849.1:c.5469G= XP_011515151.1:p.Met1823=
XM_011516850.1:c.5169G= XP_011515152.1:p.Met1723=
XM_011516851.1:c.2433G= XP_011515153.1:p.Met811=
XM_011516852.1:c.2433G= XP_011515154.1:p.Met811=
XM_011516853.1:c.5547G= XP_011515155.1:p.Met1849=
XM_011516854.1:c.1326G= XP_011515156.1:p.Met442=
XM_005250800.3:c.5547G= XP_005250857.1:p.Met1849=
XM_005250801.5:c.5547G= XP_005250858.1:p.Met1849=
XM_011516848.2:c.5544G= XP_011515150.1:p.Met1848=
XM_011516849.2:c.5469G= XP_011515151.1:p.Met1823=
XM_011516850.2:c.5169G= XP_011515152.1:p.Met1723=
XM_011516851.2:c.2433G= XP_011515153.1:p.Met811=
XM_011516852.2:c.2433G= XP_011515154.1:p.Met811=
XM_011516853.2:c.5547G= XP_011515155.1:p.Met1849=
XM_011516854.2:c.1326G= XP_011515156.1:p.Met442=
XM_017013109.1:c.5352G= XP_016868598.1:p.Met1784=
XM_017013111.1:c.2433G= XP_016868600.1:p.Met811=
XM_017013112.1:c.1104G= XP_016868601.1:p.Met368=
XM_024447074.1:c.4332G= XP_024302842.1:p.Met1444=
XR_001745482.2:n.5508G=
NM_017890.5:c.5547G= MANE Plus Clinical NP_060360.3:p.Met1849=
NM_152564.5:c.5472G= MANE Select NP_689777.3:p.Met1824=