Canonical Allele Identifier: CA371790613

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100874101G>C (hg19) ; chr8:g.99861873G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99861873G>C , CM000670.2:g.99861873G>C	GRCh38
NC_000008.10:g.100874101G>C , CM000670.1:g.100874101G>C	GRCh37
NC_000008.9:g.100943277G>C	NCBI36
NG_007098.2:g.853608G>C , LRG_351:g.853608G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*311G>C	ENSP00000507923.1:n.*311G>C
ENST00000682358.1:n.11287G>C
ENST00000683334.1:c.*6899G>C	ENSP00000507369.1:n.*6899G>C
ENST00000357162.7:c.11142G>C MANE Select	ENSP00000349685.2:p.Trp3714Cys
ENST00000358544.7:c.11217G>C MANE Plus Clinical	ENSP00000351346.2:p.Trp3739Cys
ENST00000357162.6:c.11142G>C	ENSP00000349685.2:p.Trp3714Cys
ENST00000358544.6:c.11217G>C	ENSP00000351346.2:p.Trp3739Cys
NM_017890.4:c.11217G>C , LRG_351t1:c.11217G>C	NP_060360.3:p.Trp3739Cys
NM_152564.4:c.11142G>C , LRG_351t2:c.11142G>C	NP_689777.3:p.Trp3714Cys
XM_005250800.2:c.11217G>C	XP_005250857.1:p.Trp3739Cys
XM_005250801.3:c.11217G>C	XP_005250858.1:p.Trp3739Cys
XM_011516848.1:c.11214G>C	XP_011515150.1:p.Trp3738Cys
XM_011516849.1:c.11139G>C	XP_011515151.1:p.Trp3713Cys
XM_011516850.1:c.10839G>C	XP_011515152.1:p.Trp3613Cys
XM_011516851.1:c.8103G>C	XP_011515153.1:p.Trp2701Cys
XM_011516852.1:c.8103G>C	XP_011515154.1:p.Trp2701Cys
XM_011516854.1:c.6996G>C	XP_011515156.1:p.Trp2332Cys
XM_005250800.3:c.11217G>C	XP_005250857.1:p.Trp3739Cys
XM_005250801.5:c.11217G>C	XP_005250858.1:p.Trp3739Cys
XM_011516848.2:c.11214G>C	XP_011515150.1:p.Trp3738Cys
XM_011516849.2:c.11139G>C	XP_011515151.1:p.Trp3713Cys
XM_011516850.2:c.10839G>C	XP_011515152.1:p.Trp3613Cys
XM_011516851.2:c.8103G>C	XP_011515153.1:p.Trp2701Cys
XM_011516852.2:c.8103G>C	XP_011515154.1:p.Trp2701Cys
XM_011516854.2:c.6996G>C	XP_011515156.1:p.Trp2332Cys
XM_017013109.1:c.11022G>C	XP_016868598.1:p.Trp3674Cys
XM_017013111.1:c.8103G>C	XP_016868600.1:p.Trp2701Cys
XM_017013112.1:c.6774G>C	XP_016868601.1:p.Trp2258Cys
XM_024447074.1:c.10002G>C	XP_024302842.1:p.Trp3334Cys
NM_017890.5:c.11217G>C MANE Plus Clinical	NP_060360.3:p.Trp3739Cys
NM_152564.5:c.11142G>C MANE Select	NP_689777.3:p.Trp3714Cys