Canonical Allele Identifier: CA1117129806

Gene: VPS13B

Linked Data

• dbSNP Id: rs1817224873
• gnomAD v3: 8-99868599-TAC-T
• gnomAD v4: 8-99868599-TAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868603_99868604del , CM000670.2:g.99868603_99868604del	GRCh38
NC_000008.10:g.100880831_100880832del , CM000670.1:g.100880831_100880832del	GRCh37
NC_000008.9:g.100950007_100950008del	NCBI36
NG_007098.2:g.860338_860339del , LRG_351:g.860338_860339del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*561+138_*561+139del	ENSP00000507923.1:n.*561+138_*561+139del
ENST00000682358.1:n.11537+138_11537+139del
ENST00000683334.1:c.*7149+138_*7149+139del	ENSP00000507369.1:n.*7149+138_*7149+139del
ENST00000357162.7:c.11392+138_11392+139del MANE Select	ENSP00000349685.2:n.11392+138_11392+139del
ENST00000358544.7:c.11467+138_11467+139del MANE Plus Clinical	ENSP00000351346.2:n.11467+138_11467+139del
ENST00000357162.6:c.11392+138_11392+139del	ENSP00000349685.2:n.11392+138_11392+139del
ENST00000358544.6:c.11467+138_11467+139del	ENSP00000351346.2:n.11467+138_11467+139del
ENST00000493587.1:n.409+138_409+139del
NM_017890.4:c.11467+138_11467+139del , LRG_351t1:c.11467+138_11467+139del	NP_060360.3:n.11467+138_11467+139del
NM_152564.4:c.11392+138_11392+139del , LRG_351t2:c.11392+138_11392+139del	NP_689777.3:n.11392+138_11392+139del
XM_005250800.2:c.11467+138_11467+139del	XP_005250857.1:n.11467+138_11467+139del
XM_005250801.3:c.11467+138_11467+139del	XP_005250858.1:n.11467+138_11467+139del
XM_011516848.1:c.11464+138_11464+139del	XP_011515150.1:n.11464+138_11464+139del
XM_011516849.1:c.11389+138_11389+139del	XP_011515151.1:n.11389+138_11389+139del
XM_011516850.1:c.11089+138_11089+139del	XP_011515152.1:n.11089+138_11089+139del
XM_011516851.1:c.8353+138_8353+139del	XP_011515153.1:n.8353+138_8353+139del
XM_011516852.1:c.8353+138_8353+139del	XP_011515154.1:n.8353+138_8353+139del
XM_011516854.1:c.7246+138_7246+139del	XP_011515156.1:n.7246+138_7246+139del
XM_005250800.3:c.11467+138_11467+139del	XP_005250857.1:n.11467+138_11467+139del
XM_005250801.5:c.11467+138_11467+139del	XP_005250858.1:n.11467+138_11467+139del
XM_011516848.2:c.11464+138_11464+139del	XP_011515150.1:n.11464+138_11464+139del
XM_011516849.2:c.11389+138_11389+139del	XP_011515151.1:n.11389+138_11389+139del
XM_011516850.2:c.11089+138_11089+139del	XP_011515152.1:n.11089+138_11089+139del
XM_011516851.2:c.8353+138_8353+139del	XP_011515153.1:n.8353+138_8353+139del
XM_011516852.2:c.8353+138_8353+139del	XP_011515154.1:n.8353+138_8353+139del
XM_011516854.2:c.7246+138_7246+139del	XP_011515156.1:n.7246+138_7246+139del
XM_017013109.1:c.11272+138_11272+139del	XP_016868598.1:n.11272+138_11272+139del
XM_017013111.1:c.8353+138_8353+139del	XP_016868600.1:n.8353+138_8353+139del
XM_017013112.1:c.7024+138_7024+139del	XP_016868601.1:n.7024+138_7024+139del
XM_024447074.1:c.10252+138_10252+139del	XP_024302842.1:n.10252+138_10252+139del
NM_017890.5:c.11467+138_11467+139del MANE Plus Clinical	NP_060360.3:n.11467+138_11467+139del
NM_152564.5:c.11392+138_11392+139del MANE Select	NP_689777.3:n.11392+138_11392+139del