Canonical Allele Identifier: CA1805814713
Gene: VPS13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.99699455_99699456delinsGT , CM000670.2:g.99699455_99699456delinsGT GRCh38
NC_000008.10:g.100711683_100711684delinsGT , CM000670.1:g.100711683_100711684delinsGT GRCh37
NC_000008.9:g.100780859_100780860delinsGT NCBI36
NG_007098.2:g.691190_691191delinsGT , LRG_351:g.691190_691191delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682153.1:c.6122-70_6122-69delinsGT ENSP00000507923.1:n.6122-70_6122-69delinsGT
ENST00000682358.1:n.6192-70_6192-69delinsGT
ENST00000683334.1:c.*1804-70_*1804-69delinsGT ENSP00000507369.1:n.*1804-70_*1804-69delinsGT
ENST00000357162.7:c.6047-70_6047-69delinsGT MANE Select ENSP00000349685.2:n.6047-70_6047-69delinsGT
ENST00000358544.7:c.6122-70_6122-69delinsGT MANE Plus Clinical ENSP00000351346.2:n.6122-70_6122-69delinsGT
ENST00000357162.6:c.6047-70_6047-69delinsGT ENSP00000349685.2:n.6047-70_6047-69delinsGT
ENST00000358544.6:c.6122-70_6122-69delinsGT ENSP00000351346.2:n.6122-70_6122-69delinsGT
NM_017890.4:c.6122-70_6122-69delinsGT , LRG_351t1:c.6122-70_6122-69delinsGT NP_060360.3:n.6122-70_6122-69delinsGT
NM_152564.4:c.6047-70_6047-69delinsGT , LRG_351t2:c.6047-70_6047-69delinsGT NP_689777.3:n.6047-70_6047-69delinsGT
XM_005250800.2:c.6122-70_6122-69delinsGT XP_005250857.1:n.6122-70_6122-69delinsGT
XM_005250801.3:c.6122-70_6122-69delinsGT XP_005250858.1:n.6122-70_6122-69delinsGT
XM_011516848.1:c.6119-70_6119-69delinsGT XP_011515150.1:n.6119-70_6119-69delinsGT
XM_011516849.1:c.6044-70_6044-69delinsGT XP_011515151.1:n.6044-70_6044-69delinsGT
XM_011516850.1:c.5744-70_5744-69delinsGT XP_011515152.1:n.5744-70_5744-69delinsGT
XM_011516851.1:c.3008-70_3008-69delinsGT XP_011515153.1:n.3008-70_3008-69delinsGT
XM_011516852.1:c.3008-70_3008-69delinsGT XP_011515154.1:n.3008-70_3008-69delinsGT
XM_011516853.1:c.6122-70_6122-69delinsGT XP_011515155.1:n.6122-70_6122-69delinsGT
XM_011516854.1:c.1901-70_1901-69delinsGT XP_011515156.1:n.1901-70_1901-69delinsGT
XM_005250800.3:c.6122-70_6122-69delinsGT XP_005250857.1:n.6122-70_6122-69delinsGT
XM_005250801.5:c.6122-70_6122-69delinsGT XP_005250858.1:n.6122-70_6122-69delinsGT
XM_011516848.2:c.6119-70_6119-69delinsGT XP_011515150.1:n.6119-70_6119-69delinsGT
XM_011516849.2:c.6044-70_6044-69delinsGT XP_011515151.1:n.6044-70_6044-69delinsGT
XM_011516850.2:c.5744-70_5744-69delinsGT XP_011515152.1:n.5744-70_5744-69delinsGT
XM_011516851.2:c.3008-70_3008-69delinsGT XP_011515153.1:n.3008-70_3008-69delinsGT
XM_011516852.2:c.3008-70_3008-69delinsGT XP_011515154.1:n.3008-70_3008-69delinsGT
XM_011516853.2:c.6122-70_6122-69delinsGT XP_011515155.1:n.6122-70_6122-69delinsGT
XM_011516854.2:c.1901-70_1901-69delinsGT XP_011515156.1:n.1901-70_1901-69delinsGT
XM_017013109.1:c.5927-70_5927-69delinsGT XP_016868598.1:n.5927-70_5927-69delinsGT
XM_017013111.1:c.3008-70_3008-69delinsGT XP_016868600.1:n.3008-70_3008-69delinsGT
XM_017013112.1:c.1679-70_1679-69delinsGT XP_016868601.1:n.1679-70_1679-69delinsGT
XM_024447074.1:c.4907-70_4907-69delinsGT XP_024302842.1:n.4907-70_4907-69delinsGT
XR_001745482.2:n.6083-70_6083-69delinsGT
NM_017890.5:c.6122-70_6122-69delinsGT MANE Plus Clinical NP_060360.3:n.6122-70_6122-69delinsGT
NM_152564.5:c.6047-70_6047-69delinsGT MANE Select NP_689777.3:n.6047-70_6047-69delinsGT