Canonical Allele Identifier: CA371873994

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100779045T>G (hg19) ; chr8:g.99766817T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99766817T>G , CM000670.2:g.99766817T>G	GRCh38
NC_000008.10:g.100779045T>G , CM000670.1:g.100779045T>G	GRCh37
NC_000008.9:g.100848221T>G	NCBI36
NG_007098.2:g.758552T>G , LRG_351:g.758552T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682153.1:c.7169T>G	ENSP00000507923.1:p.Phe2390Cys
ENST00000682358.1:n.7239T>G
ENST00000683334.1:c.*2851T>G	ENSP00000507369.1:n.*2851T>G
ENST00000357162.7:c.7094T>G MANE Select	ENSP00000349685.2:p.Phe2365Cys
ENST00000358544.7:c.7169T>G MANE Plus Clinical	ENSP00000351346.2:p.Phe2390Cys
ENST00000357162.6:c.7094T>G	ENSP00000349685.2:p.Phe2365Cys
ENST00000358544.6:c.7169T>G	ENSP00000351346.2:p.Phe2390Cys
ENST00000518569.1:n.224T>G
NM_017890.4:c.7169T>G , LRG_351t1:c.7169T>G	NP_060360.3:p.Phe2390Cys
NM_152564.4:c.7094T>G , LRG_351t2:c.7094T>G	NP_689777.3:p.Phe2365Cys
XM_005250800.2:c.7169T>G	XP_005250857.1:p.Phe2390Cys
XM_005250801.3:c.7169T>G	XP_005250858.1:p.Phe2390Cys
XM_011516848.1:c.7166T>G	XP_011515150.1:p.Phe2389Cys
XM_011516849.1:c.7091T>G	XP_011515151.1:p.Phe2364Cys
XM_011516850.1:c.6791T>G	XP_011515152.1:p.Phe2264Cys
XM_011516851.1:c.4055T>G	XP_011515153.1:p.Phe1352Cys
XM_011516852.1:c.4055T>G	XP_011515154.1:p.Phe1352Cys
XM_011516853.1:c.7169T>G	XP_011515155.1:p.Phe2390Cys
XM_011516854.1:c.2948T>G	XP_011515156.1:p.Phe983Cys
XR_928446.1:n.2065+3871A>C
XM_005250800.3:c.7169T>G	XP_005250857.1:p.Phe2390Cys
XM_005250801.5:c.7169T>G	XP_005250858.1:p.Phe2390Cys
XM_011516848.2:c.7166T>G	XP_011515150.1:p.Phe2389Cys
XM_011516849.2:c.7091T>G	XP_011515151.1:p.Phe2364Cys
XM_011516850.2:c.6791T>G	XP_011515152.1:p.Phe2264Cys
XM_011516851.2:c.4055T>G	XP_011515153.1:p.Phe1352Cys
XM_011516852.2:c.4055T>G	XP_011515154.1:p.Phe1352Cys
XM_011516853.2:c.7169T>G	XP_011515155.1:p.Phe2390Cys
XM_011516854.2:c.2948T>G	XP_011515156.1:p.Phe983Cys
XM_017013109.1:c.6974T>G	XP_016868598.1:p.Phe2325Cys
XM_017013111.1:c.4055T>G	XP_016868600.1:p.Phe1352Cys
XM_017013112.1:c.2726T>G	XP_016868601.1:p.Phe909Cys
XM_024447074.1:c.5954T>G	XP_024302842.1:p.Phe1985Cys
NM_017890.5:c.7169T>G MANE Plus Clinical	NP_060360.3:p.Phe2390Cys
NM_152564.5:c.7094T>G MANE Select	NP_689777.3:p.Phe2365Cys