Canonical Allele Identifier: CA371782914

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100847544A>G (hg19) ; chr8:g.99835316A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99835316A>G , CM000670.2:g.99835316A>G	GRCh38
NC_000008.10:g.100847544A>G , CM000670.1:g.100847544A>G	GRCh37
NC_000008.9:g.100916720A>G	NCBI36
NG_007098.2:g.827051A>G , LRG_351:g.827051A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682153.1:c.9809A>G	ENSP00000507923.1:p.Asn3270Ser
ENST00000682358.1:n.9879A>G
ENST00000683334.1:c.*5491A>G	ENSP00000507369.1:n.*5491A>G
ENST00000357162.7:c.9734A>G MANE Select	ENSP00000349685.2:p.Asn3245Ser
ENST00000358544.7:c.9809A>G MANE Plus Clinical	ENSP00000351346.2:p.Asn3270Ser
ENST00000357162.6:c.9734A>G	ENSP00000349685.2:p.Asn3245Ser
ENST00000358544.6:c.9809A>G	ENSP00000351346.2:p.Asn3270Ser
NM_017890.4:c.9809A>G , LRG_351t1:c.9809A>G	NP_060360.3:p.Asn3270Ser
NM_152564.4:c.9734A>G , LRG_351t2:c.9734A>G	NP_689777.3:p.Asn3245Ser
XM_005250800.2:c.9809A>G	XP_005250857.1:p.Asn3270Ser
XM_005250801.3:c.9809A>G	XP_005250858.1:p.Asn3270Ser
XM_011516848.1:c.9806A>G	XP_011515150.1:p.Asn3269Ser
XM_011516849.1:c.9731A>G	XP_011515151.1:p.Asn3244Ser
XM_011516850.1:c.9431A>G	XP_011515152.1:p.Asn3144Ser
XM_011516851.1:c.6695A>G	XP_011515153.1:p.Asn2232Ser
XM_011516852.1:c.6695A>G	XP_011515154.1:p.Asn2232Ser
XM_011516854.1:c.5588A>G	XP_011515156.1:p.Asn1863Ser
XM_005250800.3:c.9809A>G	XP_005250857.1:p.Asn3270Ser
XM_005250801.5:c.9809A>G	XP_005250858.1:p.Asn3270Ser
XM_011516848.2:c.9806A>G	XP_011515150.1:p.Asn3269Ser
XM_011516849.2:c.9731A>G	XP_011515151.1:p.Asn3244Ser
XM_011516850.2:c.9431A>G	XP_011515152.1:p.Asn3144Ser
XM_011516851.2:c.6695A>G	XP_011515153.1:p.Asn2232Ser
XM_011516852.2:c.6695A>G	XP_011515154.1:p.Asn2232Ser
XM_011516854.2:c.5588A>G	XP_011515156.1:p.Asn1863Ser
XM_017013109.1:c.9614A>G	XP_016868598.1:p.Asn3205Ser
XM_017013111.1:c.6695A>G	XP_016868600.1:p.Asn2232Ser
XM_017013112.1:c.5366A>G	XP_016868601.1:p.Asn1789Ser
XM_024447074.1:c.8594A>G	XP_024302842.1:p.Asn2865Ser
NM_017890.5:c.9809A>G MANE Plus Clinical	NP_060360.3:p.Asn3270Ser
NM_152564.5:c.9734A>G MANE Select	NP_689777.3:p.Asn3245Ser