Canonical Allele Identifier: CA462338275

Gene: VPS13B

Linked Data

• gnomAD v4: 8-99861888-C-A
• MyVariant Identifiers: chr8:g.100874116C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99861888C>A , CM000670.2:g.99861888C>A	GRCh38
NC_000008.10:g.100874116C>A , CM000670.1:g.100874116C>A	GRCh37
NC_000008.9:g.100943292C>A	NCBI36
NG_007098.2:g.853623C>A , LRG_351:g.853623C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*326C>A	ENSP00000507923.1:n.*326C>A
ENST00000682358.1:n.11302C>A
ENST00000683334.1:c.*6914C>A	ENSP00000507369.1:n.*6914C>A
ENST00000357162.7:c.11157C>A MANE Select	ENSP00000349685.2:p.Pro3719=
ENST00000358544.7:c.11232C>A MANE Plus Clinical	ENSP00000351346.2:p.Pro3744=
ENST00000357162.6:c.11157C>A	ENSP00000349685.2:p.Pro3719=
ENST00000358544.6:c.11232C>A	ENSP00000351346.2:p.Pro3744=
NM_017890.4:c.11232C>A , LRG_351t1:c.11232C>A	NP_060360.3:p.Pro3744=
NM_152564.4:c.11157C>A , LRG_351t2:c.11157C>A	NP_689777.3:p.Pro3719=
XM_005250800.2:c.11232C>A	XP_005250857.1:p.Pro3744=
XM_005250801.3:c.11232C>A	XP_005250858.1:p.Pro3744=
XM_011516848.1:c.11229C>A	XP_011515150.1:p.Pro3743=
XM_011516849.1:c.11154C>A	XP_011515151.1:p.Pro3718=
XM_011516850.1:c.10854C>A	XP_011515152.1:p.Pro3618=
XM_011516851.1:c.8118C>A	XP_011515153.1:p.Pro2706=
XM_011516852.1:c.8118C>A	XP_011515154.1:p.Pro2706=
XM_011516854.1:c.7011C>A	XP_011515156.1:p.Pro2337=
XM_005250800.3:c.11232C>A	XP_005250857.1:p.Pro3744=
XM_005250801.5:c.11232C>A	XP_005250858.1:p.Pro3744=
XM_011516848.2:c.11229C>A	XP_011515150.1:p.Pro3743=
XM_011516849.2:c.11154C>A	XP_011515151.1:p.Pro3718=
XM_011516850.2:c.10854C>A	XP_011515152.1:p.Pro3618=
XM_011516851.2:c.8118C>A	XP_011515153.1:p.Pro2706=
XM_011516852.2:c.8118C>A	XP_011515154.1:p.Pro2706=
XM_011516854.2:c.7011C>A	XP_011515156.1:p.Pro2337=
XM_017013109.1:c.11037C>A	XP_016868598.1:p.Pro3679=
XM_017013111.1:c.8118C>A	XP_016868600.1:p.Pro2706=
XM_017013112.1:c.6789C>A	XP_016868601.1:p.Pro2263=
XM_024447074.1:c.10017C>A	XP_024302842.1:p.Pro3339=
NM_017890.5:c.11232C>A MANE Plus Clinical	NP_060360.3:p.Pro3744=
NM_152564.5:c.11157C>A MANE Select	NP_689777.3:p.Pro3719=