Canonical Allele Identifier: CA462440267

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100729505C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99717277C>T , CM000670.2:g.99717277C>T	GRCh38
NC_000008.10:g.100729505C>T , CM000670.1:g.100729505C>T	GRCh37
NC_000008.9:g.100798681C>T	NCBI36
NG_007098.2:g.709012C>T , LRG_351:g.709012C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682153.1:c.6636C>T	ENSP00000507923.1:p.Ala2212=
ENST00000682358.1:n.6706C>T
ENST00000683334.1:c.*2318C>T	ENSP00000507369.1:n.*2318C>T
ENST00000357162.7:c.6561C>T MANE Select	ENSP00000349685.2:p.Ala2187=
ENST00000358544.7:c.6636C>T MANE Plus Clinical	ENSP00000351346.2:p.Ala2212=
ENST00000357162.6:c.6561C>T	ENSP00000349685.2:p.Ala2187=
ENST00000358544.6:c.6636C>T	ENSP00000351346.2:p.Ala2212=
NM_017890.4:c.6636C>T , LRG_351t1:c.6636C>T	NP_060360.3:p.Ala2212=
NM_152564.4:c.6561C>T , LRG_351t2:c.6561C>T	NP_689777.3:p.Ala2187=
XM_005250800.2:c.6636C>T	XP_005250857.1:p.Ala2212=
XM_005250801.3:c.6636C>T	XP_005250858.1:p.Ala2212=
XM_011516848.1:c.6633C>T	XP_011515150.1:p.Ala2211=
XM_011516849.1:c.6558C>T	XP_011515151.1:p.Ala2186=
XM_011516850.1:c.6258C>T	XP_011515152.1:p.Ala2086=
XM_011516851.1:c.3522C>T	XP_011515153.1:p.Ala1174=
XM_011516852.1:c.3522C>T	XP_011515154.1:p.Ala1174=
XM_011516853.1:c.6636C>T	XP_011515155.1:p.Ala2212=
XM_011516854.1:c.2415C>T	XP_011515156.1:p.Ala805=
XM_005250800.3:c.6636C>T	XP_005250857.1:p.Ala2212=
XM_005250801.5:c.6636C>T	XP_005250858.1:p.Ala2212=
XM_011516848.2:c.6633C>T	XP_011515150.1:p.Ala2211=
XM_011516849.2:c.6558C>T	XP_011515151.1:p.Ala2186=
XM_011516850.2:c.6258C>T	XP_011515152.1:p.Ala2086=
XM_011516851.2:c.3522C>T	XP_011515153.1:p.Ala1174=
XM_011516852.2:c.3522C>T	XP_011515154.1:p.Ala1174=
XM_011516853.2:c.6636C>T	XP_011515155.1:p.Ala2212=
XM_011516854.2:c.2415C>T	XP_011515156.1:p.Ala805=
XM_017013109.1:c.6441C>T	XP_016868598.1:p.Ala2147=
XM_017013111.1:c.3522C>T	XP_016868600.1:p.Ala1174=
XM_017013112.1:c.2193C>T	XP_016868601.1:p.Ala731=
XM_024447074.1:c.5421C>T	XP_024302842.1:p.Ala1807=
NM_017890.5:c.6636C>T MANE Plus Clinical	NP_060360.3:p.Ala2212=
NM_152564.5:c.6561C>T MANE Select	NP_689777.3:p.Ala2187=