Canonical Allele Identifier: CA371875749
Gene: VPS13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.99776877T>A , CM000670.2:g.99776877T>A GRCh38
NC_000008.10:g.100789105T>A , CM000670.1:g.100789105T>A GRCh37
NC_000008.9:g.100858281T>A NCBI36
NG_007098.2:g.768612T>A , LRG_351:g.768612T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682153.1:c.7425T>A ENSP00000507923.1:p.Phe2475Leu
ENST00000682358.1:n.7495T>A
ENST00000683334.1:c.*3107T>A ENSP00000507369.1:n.*3107T>A
ENST00000357162.7:c.7350T>A MANE Select ENSP00000349685.2:p.Phe2450Leu
ENST00000358544.7:c.7425T>A MANE Plus Clinical ENSP00000351346.2:p.Phe2475Leu
ENST00000357162.6:c.7350T>A ENSP00000349685.2:p.Phe2450Leu
ENST00000358544.6:c.7425T>A ENSP00000351346.2:p.Phe2475Leu
ENST00000518569.1:n.378-1805T>A
NM_017890.4:c.7425T>A , LRG_351t1:c.7425T>A NP_060360.3:p.Phe2475Leu
NM_152564.4:c.7350T>A , LRG_351t2:c.7350T>A NP_689777.3:p.Phe2450Leu
XM_005250800.2:c.7425T>A XP_005250857.1:p.Phe2475Leu
XM_005250801.3:c.7425T>A XP_005250858.1:p.Phe2475Leu
XM_011516848.1:c.7422T>A XP_011515150.1:p.Phe2474Leu
XM_011516849.1:c.7347T>A XP_011515151.1:p.Phe2449Leu
XM_011516850.1:c.7047T>A XP_011515152.1:p.Phe2349Leu
XM_011516851.1:c.4311T>A XP_011515153.1:p.Phe1437Leu
XM_011516852.1:c.4311T>A XP_011515154.1:p.Phe1437Leu
XM_011516853.1:c.7425T>A XP_011515155.1:p.Phe2475Leu
XM_011516854.1:c.3204T>A XP_011515156.1:p.Phe1068Leu
XR_928446.1:n.1830+5601A>T
XM_005250800.3:c.7425T>A XP_005250857.1:p.Phe2475Leu
XM_005250801.5:c.7425T>A XP_005250858.1:p.Phe2475Leu
XM_011516848.2:c.7422T>A XP_011515150.1:p.Phe2474Leu
XM_011516849.2:c.7347T>A XP_011515151.1:p.Phe2449Leu
XM_011516850.2:c.7047T>A XP_011515152.1:p.Phe2349Leu
XM_011516851.2:c.4311T>A XP_011515153.1:p.Phe1437Leu
XM_011516852.2:c.4311T>A XP_011515154.1:p.Phe1437Leu
XM_011516853.2:c.7425T>A XP_011515155.1:p.Phe2475Leu
XM_011516854.2:c.3204T>A XP_011515156.1:p.Phe1068Leu
XM_017013109.1:c.7230T>A XP_016868598.1:p.Phe2410Leu
XM_017013111.1:c.4311T>A XP_016868600.1:p.Phe1437Leu
XM_017013112.1:c.2982T>A XP_016868601.1:p.Phe994Leu
XM_024447074.1:c.6210T>A XP_024302842.1:p.Phe2070Leu
NM_017890.5:c.7425T>A MANE Plus Clinical NP_060360.3:p.Phe2475Leu
NM_152564.5:c.7350T>A MANE Select NP_689777.3:p.Phe2450Leu