Canonical Allele Identifier: CA16041240
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 370884
ClinVar RCV Id: RCV000410909
dbSNP Id: rs1057516841

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.99699520_99699525del , CM000670.2:g.99699520_99699525del GRCh38
NC_000008.10:g.100711748_100711753del , CM000670.1:g.100711748_100711753del GRCh37
NC_000008.9:g.100780924_100780929del NCBI36
NG_007098.2:g.691255_691260del , LRG_351:g.691255_691260del

Transcript Alleles

HGVS Amino-acid change
ENST00000682153.1:c.6122-5_6122del
ENST00000682358.1:n.6192-5_6192del
ENST00000683334.1:c.*1804-5_*1804del
ENST00000357162.7:c.6047-5_6047del
ENST00000358544.7:c.6122-5_6122del
ENST00000357162.6:c.6047-5_6047del
ENST00000358544.6:c.6122-5_6122del
NM_017890.4:c.6122-5_6122del , LRG_351t1:c.6122-5_6122del
NM_152564.4:c.6047-5_6047del , LRG_351t2:c.6047-5_6047del
XM_005250800.2:c.6122-5_6122del
XM_005250801.3:c.6122-5_6122del
XM_011516848.1:c.6119-5_6119del
XM_011516849.1:c.6044-5_6044del
XM_011516850.1:c.5744-5_5744del
XM_011516851.1:c.3008-5_3008del
XM_011516852.1:c.3008-5_3008del
XM_011516853.1:c.6122-5_6122del
XM_011516854.1:c.1901-5_1901del
XM_005250800.3:c.6122-5_6122del
XM_005250801.5:c.6122-5_6122del
XM_011516848.2:c.6119-5_6119del
XM_011516849.2:c.6044-5_6044del
XM_011516850.2:c.5744-5_5744del
XM_011516851.2:c.3008-5_3008del
XM_011516852.2:c.3008-5_3008del
XM_011516853.2:c.6122-5_6122del
XM_011516854.2:c.1901-5_1901del
XM_017013109.1:c.5927-5_5927del
XM_017013111.1:c.3008-5_3008del
XM_017013112.1:c.1679-5_1679del
XM_024447074.1:c.4907-5_4907del
XR_001745482.2:n.6083-5_6083del
NM_017890.5:c.6122-5_6122del
NM_152564.5:c.6047-5_6047del