Canonical Allele Identifier: CA371790675

Gene: VPS13B

Linked Data

• gnomAD v4: 8-99861899-G-T
• MyVariant Identifiers: chr8:g.100874127G>T (hg19) ; chr8:g.99861899G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99861899G>T , CM000670.2:g.99861899G>T	GRCh38
NC_000008.10:g.100874127G>T , CM000670.1:g.100874127G>T	GRCh37
NC_000008.9:g.100943303G>T	NCBI36
NG_007098.2:g.853634G>T , LRG_351:g.853634G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*337G>T	ENSP00000507923.1:n.*337G>T
ENST00000682358.1:n.11313G>T
ENST00000683334.1:c.*6925G>T	ENSP00000507369.1:n.*6925G>T
ENST00000357162.7:c.11168G>T MANE Select	ENSP00000349685.2:p.Gly3723Val
ENST00000358544.7:c.11243G>T MANE Plus Clinical	ENSP00000351346.2:p.Gly3748Val
ENST00000357162.6:c.11168G>T	ENSP00000349685.2:p.Gly3723Val
ENST00000358544.6:c.11243G>T	ENSP00000351346.2:p.Gly3748Val
NM_017890.4:c.11243G>T , LRG_351t1:c.11243G>T	NP_060360.3:p.Gly3748Val
NM_152564.4:c.11168G>T , LRG_351t2:c.11168G>T	NP_689777.3:p.Gly3723Val
XM_005250800.2:c.11243G>T	XP_005250857.1:p.Gly3748Val
XM_005250801.3:c.11243G>T	XP_005250858.1:p.Gly3748Val
XM_011516848.1:c.11240G>T	XP_011515150.1:p.Gly3747Val
XM_011516849.1:c.11165G>T	XP_011515151.1:p.Gly3722Val
XM_011516850.1:c.10865G>T	XP_011515152.1:p.Gly3622Val
XM_011516851.1:c.8129G>T	XP_011515153.1:p.Gly2710Val
XM_011516852.1:c.8129G>T	XP_011515154.1:p.Gly2710Val
XM_011516854.1:c.7022G>T	XP_011515156.1:p.Gly2341Val
XM_005250800.3:c.11243G>T	XP_005250857.1:p.Gly3748Val
XM_005250801.5:c.11243G>T	XP_005250858.1:p.Gly3748Val
XM_011516848.2:c.11240G>T	XP_011515150.1:p.Gly3747Val
XM_011516849.2:c.11165G>T	XP_011515151.1:p.Gly3722Val
XM_011516850.2:c.10865G>T	XP_011515152.1:p.Gly3622Val
XM_011516851.2:c.8129G>T	XP_011515153.1:p.Gly2710Val
XM_011516852.2:c.8129G>T	XP_011515154.1:p.Gly2710Val
XM_011516854.2:c.7022G>T	XP_011515156.1:p.Gly2341Val
XM_017013109.1:c.11048G>T	XP_016868598.1:p.Gly3683Val
XM_017013111.1:c.8129G>T	XP_016868600.1:p.Gly2710Val
XM_017013112.1:c.6800G>T	XP_016868601.1:p.Gly2267Val
XM_024447074.1:c.10028G>T	XP_024302842.1:p.Gly3343Val
NM_017890.5:c.11243G>T MANE Plus Clinical	NP_060360.3:p.Gly3748Val
NM_152564.5:c.11168G>T MANE Select	NP_689777.3:p.Gly3723Val