Canonical Allele Identifier: CA371785714

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100866359A>C (hg19) ; chr8:g.99854131A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99854131A>C , CM000670.2:g.99854131A>C	GRCh38
NC_000008.10:g.100866359A>C , CM000670.1:g.100866359A>C	GRCh37
NC_000008.9:g.100935535A>C	NCBI36
NG_007098.2:g.845866A>C , LRG_351:g.845866A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682153.1:c.10817A>C	ENSP00000507923.1:p.Tyr3606Ser
ENST00000682358.1:n.10887A>C
ENST00000683334.1:c.*6499A>C	ENSP00000507369.1:n.*6499A>C
ENST00000357162.7:c.10742A>C MANE Select	ENSP00000349685.2:p.Tyr3581Ser
ENST00000358544.7:c.10817A>C MANE Plus Clinical	ENSP00000351346.2:p.Tyr3606Ser
ENST00000357162.6:c.10742A>C	ENSP00000349685.2:p.Tyr3581Ser
ENST00000358544.6:c.10817A>C	ENSP00000351346.2:p.Tyr3606Ser
NM_017890.4:c.10817A>C , LRG_351t1:c.10817A>C	NP_060360.3:p.Tyr3606Ser
NM_152564.4:c.10742A>C , LRG_351t2:c.10742A>C	NP_689777.3:p.Tyr3581Ser
XM_005250800.2:c.10817A>C	XP_005250857.1:p.Tyr3606Ser
XM_005250801.3:c.10817A>C	XP_005250858.1:p.Tyr3606Ser
XM_011516848.1:c.10814A>C	XP_011515150.1:p.Tyr3605Ser
XM_011516849.1:c.10739A>C	XP_011515151.1:p.Tyr3580Ser
XM_011516850.1:c.10439A>C	XP_011515152.1:p.Tyr3480Ser
XM_011516851.1:c.7703A>C	XP_011515153.1:p.Tyr2568Ser
XM_011516852.1:c.7703A>C	XP_011515154.1:p.Tyr2568Ser
XM_011516854.1:c.6596A>C	XP_011515156.1:p.Tyr2199Ser
XM_005250800.3:c.10817A>C	XP_005250857.1:p.Tyr3606Ser
XM_005250801.5:c.10817A>C	XP_005250858.1:p.Tyr3606Ser
XM_011516848.2:c.10814A>C	XP_011515150.1:p.Tyr3605Ser
XM_011516849.2:c.10739A>C	XP_011515151.1:p.Tyr3580Ser
XM_011516850.2:c.10439A>C	XP_011515152.1:p.Tyr3480Ser
XM_011516851.2:c.7703A>C	XP_011515153.1:p.Tyr2568Ser
XM_011516852.2:c.7703A>C	XP_011515154.1:p.Tyr2568Ser
XM_011516854.2:c.6596A>C	XP_011515156.1:p.Tyr2199Ser
XM_017013109.1:c.10622A>C	XP_016868598.1:p.Tyr3541Ser
XM_017013111.1:c.7703A>C	XP_016868600.1:p.Tyr2568Ser
XM_017013112.1:c.6374A>C	XP_016868601.1:p.Tyr2125Ser
XM_024447074.1:c.9602A>C	XP_024302842.1:p.Tyr3201Ser
NM_017890.5:c.10817A>C MANE Plus Clinical	NP_060360.3:p.Tyr3606Ser
NM_152564.5:c.10742A>C MANE Select	NP_689777.3:p.Tyr3581Ser