Canonical Allele Identifier: CA371790264

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100874026C>G (hg19) ; chr8:g.99861798C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99861798C>G , CM000670.2:g.99861798C>G	GRCh38
NC_000008.10:g.100874026C>G , CM000670.1:g.100874026C>G	GRCh37
NC_000008.9:g.100943202C>G	NCBI36
NG_007098.2:g.853533C>G , LRG_351:g.853533C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*236C>G	ENSP00000507923.1:n.*236C>G
ENST00000682358.1:n.11212C>G
ENST00000683334.1:c.*6824C>G	ENSP00000507369.1:n.*6824C>G
ENST00000357162.7:c.11067C>G MANE Select	ENSP00000349685.2:p.Asn3689Lys
ENST00000358544.7:c.11142C>G MANE Plus Clinical	ENSP00000351346.2:p.Asn3714Lys
ENST00000357162.6:c.11067C>G	ENSP00000349685.2:p.Asn3689Lys
ENST00000358544.6:c.11142C>G	ENSP00000351346.2:p.Asn3714Lys
NM_017890.4:c.11142C>G , LRG_351t1:c.11142C>G	NP_060360.3:p.Asn3714Lys
NM_152564.4:c.11067C>G , LRG_351t2:c.11067C>G	NP_689777.3:p.Asn3689Lys
XM_005250800.2:c.11142C>G	XP_005250857.1:p.Asn3714Lys
XM_005250801.3:c.11142C>G	XP_005250858.1:p.Asn3714Lys
XM_011516848.1:c.11139C>G	XP_011515150.1:p.Asn3713Lys
XM_011516849.1:c.11064C>G	XP_011515151.1:p.Asn3688Lys
XM_011516850.1:c.10764C>G	XP_011515152.1:p.Asn3588Lys
XM_011516851.1:c.8028C>G	XP_011515153.1:p.Asn2676Lys
XM_011516852.1:c.8028C>G	XP_011515154.1:p.Asn2676Lys
XM_011516854.1:c.6921C>G	XP_011515156.1:p.Asn2307Lys
XM_005250800.3:c.11142C>G	XP_005250857.1:p.Asn3714Lys
XM_005250801.5:c.11142C>G	XP_005250858.1:p.Asn3714Lys
XM_011516848.2:c.11139C>G	XP_011515150.1:p.Asn3713Lys
XM_011516849.2:c.11064C>G	XP_011515151.1:p.Asn3688Lys
XM_011516850.2:c.10764C>G	XP_011515152.1:p.Asn3588Lys
XM_011516851.2:c.8028C>G	XP_011515153.1:p.Asn2676Lys
XM_011516852.2:c.8028C>G	XP_011515154.1:p.Asn2676Lys
XM_011516854.2:c.6921C>G	XP_011515156.1:p.Asn2307Lys
XM_017013109.1:c.10947C>G	XP_016868598.1:p.Asn3649Lys
XM_017013111.1:c.8028C>G	XP_016868600.1:p.Asn2676Lys
XM_017013112.1:c.6699C>G	XP_016868601.1:p.Asn2233Lys
XM_024447074.1:c.9927C>G	XP_024302842.1:p.Asn3309Lys
NM_017890.5:c.11142C>G MANE Plus Clinical	NP_060360.3:p.Asn3714Lys
NM_152564.5:c.11067C>G MANE Select	NP_689777.3:p.Asn3689Lys