Canonical Allele Identifier: CA371875613

Gene: VPS13B

Linked Data

• gnomAD v4: 8-99776810-A-G
• MyVariant Identifiers: chr8:g.100789038A>G (hg19) ; chr8:g.99776810A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99776810A>G , CM000670.2:g.99776810A>G	GRCh38
NC_000008.10:g.100789038A>G , CM000670.1:g.100789038A>G	GRCh37
NC_000008.9:g.100858214A>G	NCBI36
NG_007098.2:g.768545A>G , LRG_351:g.768545A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.7358A>G	ENSP00000507923.1:p.Asp2453Gly
ENST00000682358.1:n.7428A>G
ENST00000683334.1:c.*3040A>G	ENSP00000507369.1:n.*3040A>G
ENST00000357162.7:c.7283A>G MANE Select	ENSP00000349685.2:p.Asp2428Gly
ENST00000358544.7:c.7358A>G MANE Plus Clinical	ENSP00000351346.2:p.Asp2453Gly
ENST00000357162.6:c.7283A>G	ENSP00000349685.2:p.Asp2428Gly
ENST00000358544.6:c.7358A>G	ENSP00000351346.2:p.Asp2453Gly
ENST00000518569.1:n.378-1872A>G
NM_017890.4:c.7358A>G , LRG_351t1:c.7358A>G	NP_060360.3:p.Asp2453Gly
NM_152564.4:c.7283A>G , LRG_351t2:c.7283A>G	NP_689777.3:p.Asp2428Gly
XM_005250800.2:c.7358A>G	XP_005250857.1:p.Asp2453Gly
XM_005250801.3:c.7358A>G	XP_005250858.1:p.Asp2453Gly
XM_011516848.1:c.7355A>G	XP_011515150.1:p.Asp2452Gly
XM_011516849.1:c.7280A>G	XP_011515151.1:p.Asp2427Gly
XM_011516850.1:c.6980A>G	XP_011515152.1:p.Asp2327Gly
XM_011516851.1:c.4244A>G	XP_011515153.1:p.Asp1415Gly
XM_011516852.1:c.4244A>G	XP_011515154.1:p.Asp1415Gly
XM_011516853.1:c.7358A>G	XP_011515155.1:p.Asp2453Gly
XM_011516854.1:c.3137A>G	XP_011515156.1:p.Asp1046Gly
XR_928446.1:n.1830+5668T>C
XM_005250800.3:c.7358A>G	XP_005250857.1:p.Asp2453Gly
XM_005250801.5:c.7358A>G	XP_005250858.1:p.Asp2453Gly
XM_011516848.2:c.7355A>G	XP_011515150.1:p.Asp2452Gly
XM_011516849.2:c.7280A>G	XP_011515151.1:p.Asp2427Gly
XM_011516850.2:c.6980A>G	XP_011515152.1:p.Asp2327Gly
XM_011516851.2:c.4244A>G	XP_011515153.1:p.Asp1415Gly
XM_011516852.2:c.4244A>G	XP_011515154.1:p.Asp1415Gly
XM_011516853.2:c.7358A>G	XP_011515155.1:p.Asp2453Gly
XM_011516854.2:c.3137A>G	XP_011515156.1:p.Asp1046Gly
XM_017013109.1:c.7163A>G	XP_016868598.1:p.Asp2388Gly
XM_017013111.1:c.4244A>G	XP_016868600.1:p.Asp1415Gly
XM_017013112.1:c.2915A>G	XP_016868601.1:p.Asp972Gly
XM_024447074.1:c.6143A>G	XP_024302842.1:p.Asp2048Gly
NM_017890.5:c.7358A>G MANE Plus Clinical	NP_060360.3:p.Asp2453Gly
NM_152564.5:c.7283A>G MANE Select	NP_689777.3:p.Asp2428Gly