Canonical Allele Identifier: CA371792533

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100880691A>T (hg19) ; chr8:g.99868463A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868463A>T , CM000670.2:g.99868463A>T	GRCh38
NC_000008.10:g.100880691A>T , CM000670.1:g.100880691A>T	GRCh37
NC_000008.9:g.100949867A>T	NCBI36
NG_007098.2:g.860198A>T , LRG_351:g.860198A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*559A>T	ENSP00000507923.1:n.*559A>T
ENST00000682358.1:n.11535A>T
ENST00000683334.1:c.*7147A>T	ENSP00000507369.1:n.*7147A>T
ENST00000357162.7:c.11390A>T MANE Select	ENSP00000349685.2:p.Tyr3797Phe
ENST00000358544.7:c.11465A>T MANE Plus Clinical	ENSP00000351346.2:p.Tyr3822Phe
ENST00000357162.6:c.11390A>T	ENSP00000349685.2:p.Tyr3797Phe
ENST00000358544.6:c.11465A>T	ENSP00000351346.2:p.Tyr3822Phe
ENST00000493587.1:n.407A>T
NM_017890.4:c.11465A>T , LRG_351t1:c.11465A>T	NP_060360.3:p.Tyr3822Phe
NM_152564.4:c.11390A>T , LRG_351t2:c.11390A>T	NP_689777.3:p.Tyr3797Phe
XM_005250800.2:c.11465A>T	XP_005250857.1:p.Tyr3822Phe
XM_005250801.3:c.11465A>T	XP_005250858.1:p.Tyr3822Phe
XM_011516848.1:c.11462A>T	XP_011515150.1:p.Tyr3821Phe
XM_011516849.1:c.11387A>T	XP_011515151.1:p.Tyr3796Phe
XM_011516850.1:c.11087A>T	XP_011515152.1:p.Tyr3696Phe
XM_011516851.1:c.8351A>T	XP_011515153.1:p.Tyr2784Phe
XM_011516852.1:c.8351A>T	XP_011515154.1:p.Tyr2784Phe
XM_011516854.1:c.7244A>T	XP_011515156.1:p.Tyr2415Phe
XM_005250800.3:c.11465A>T	XP_005250857.1:p.Tyr3822Phe
XM_005250801.5:c.11465A>T	XP_005250858.1:p.Tyr3822Phe
XM_011516848.2:c.11462A>T	XP_011515150.1:p.Tyr3821Phe
XM_011516849.2:c.11387A>T	XP_011515151.1:p.Tyr3796Phe
XM_011516850.2:c.11087A>T	XP_011515152.1:p.Tyr3696Phe
XM_011516851.2:c.8351A>T	XP_011515153.1:p.Tyr2784Phe
XM_011516852.2:c.8351A>T	XP_011515154.1:p.Tyr2784Phe
XM_011516854.2:c.7244A>T	XP_011515156.1:p.Tyr2415Phe
XM_017013109.1:c.11270A>T	XP_016868598.1:p.Tyr3757Phe
XM_017013111.1:c.8351A>T	XP_016868600.1:p.Tyr2784Phe
XM_017013112.1:c.7022A>T	XP_016868601.1:p.Tyr2341Phe
XM_024447074.1:c.10250A>T	XP_024302842.1:p.Tyr3417Phe
NM_017890.5:c.11465A>T MANE Plus Clinical	NP_060360.3:p.Tyr3822Phe
NM_152564.5:c.11390A>T MANE Select	NP_689777.3:p.Tyr3797Phe