Canonical Allele Identifier: CA462338070

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100874065A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99861837A>T , CM000670.2:g.99861837A>T	GRCh38
NC_000008.10:g.100874065A>T , CM000670.1:g.100874065A>T	GRCh37
NC_000008.9:g.100943241A>T	NCBI36
NG_007098.2:g.853572A>T , LRG_351:g.853572A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682153.1:c.*275A>T	ENSP00000507923.1:n.*275A>T
ENST00000682358.1:n.11251A>T
ENST00000683334.1:c.*6863A>T	ENSP00000507369.1:n.*6863A>T
ENST00000357162.7:c.11106A>T MANE Select	ENSP00000349685.2:p.Ser3702=
ENST00000358544.7:c.11181A>T MANE Plus Clinical	ENSP00000351346.2:p.Ser3727=
ENST00000357162.6:c.11106A>T	ENSP00000349685.2:p.Ser3702=
ENST00000358544.6:c.11181A>T	ENSP00000351346.2:p.Ser3727=
NM_017890.4:c.11181A>T , LRG_351t1:c.11181A>T	NP_060360.3:p.Ser3727=
NM_152564.4:c.11106A>T , LRG_351t2:c.11106A>T	NP_689777.3:p.Ser3702=
XM_005250800.2:c.11181A>T	XP_005250857.1:p.Ser3727=
XM_005250801.3:c.11181A>T	XP_005250858.1:p.Ser3727=
XM_011516848.1:c.11178A>T	XP_011515150.1:p.Ser3726=
XM_011516849.1:c.11103A>T	XP_011515151.1:p.Ser3701=
XM_011516850.1:c.10803A>T	XP_011515152.1:p.Ser3601=
XM_011516851.1:c.8067A>T	XP_011515153.1:p.Ser2689=
XM_011516852.1:c.8067A>T	XP_011515154.1:p.Ser2689=
XM_011516854.1:c.6960A>T	XP_011515156.1:p.Ser2320=
XM_005250800.3:c.11181A>T	XP_005250857.1:p.Ser3727=
XM_005250801.5:c.11181A>T	XP_005250858.1:p.Ser3727=
XM_011516848.2:c.11178A>T	XP_011515150.1:p.Ser3726=
XM_011516849.2:c.11103A>T	XP_011515151.1:p.Ser3701=
XM_011516850.2:c.10803A>T	XP_011515152.1:p.Ser3601=
XM_011516851.2:c.8067A>T	XP_011515153.1:p.Ser2689=
XM_011516852.2:c.8067A>T	XP_011515154.1:p.Ser2689=
XM_011516854.2:c.6960A>T	XP_011515156.1:p.Ser2320=
XM_017013109.1:c.10986A>T	XP_016868598.1:p.Ser3662=
XM_017013111.1:c.8067A>T	XP_016868600.1:p.Ser2689=
XM_017013112.1:c.6738A>T	XP_016868601.1:p.Ser2246=
XM_024447074.1:c.9966A>T	XP_024302842.1:p.Ser3322=
NM_017890.5:c.11181A>T MANE Plus Clinical	NP_060360.3:p.Ser3727=
NM_152564.5:c.11106A>T MANE Select	NP_689777.3:p.Ser3702=