Canonical Allele Identifier: CA371790517

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100874082A>C (hg19) ; chr8:g.99861854A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99861854A>C , CM000670.2:g.99861854A>C	GRCh38
NC_000008.10:g.100874082A>C , CM000670.1:g.100874082A>C	GRCh37
NC_000008.9:g.100943258A>C	NCBI36
NG_007098.2:g.853589A>C , LRG_351:g.853589A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*292A>C	ENSP00000507923.1:n.*292A>C
ENST00000682358.1:n.11268A>C
ENST00000683334.1:c.*6880A>C	ENSP00000507369.1:n.*6880A>C
ENST00000357162.7:c.11123A>C MANE Select	ENSP00000349685.2:p.Tyr3708Ser
ENST00000358544.7:c.11198A>C MANE Plus Clinical	ENSP00000351346.2:p.Tyr3733Ser
ENST00000357162.6:c.11123A>C	ENSP00000349685.2:p.Tyr3708Ser
ENST00000358544.6:c.11198A>C	ENSP00000351346.2:p.Tyr3733Ser
NM_017890.4:c.11198A>C , LRG_351t1:c.11198A>C	NP_060360.3:p.Tyr3733Ser
NM_152564.4:c.11123A>C , LRG_351t2:c.11123A>C	NP_689777.3:p.Tyr3708Ser
XM_005250800.2:c.11198A>C	XP_005250857.1:p.Tyr3733Ser
XM_005250801.3:c.11198A>C	XP_005250858.1:p.Tyr3733Ser
XM_011516848.1:c.11195A>C	XP_011515150.1:p.Tyr3732Ser
XM_011516849.1:c.11120A>C	XP_011515151.1:p.Tyr3707Ser
XM_011516850.1:c.10820A>C	XP_011515152.1:p.Tyr3607Ser
XM_011516851.1:c.8084A>C	XP_011515153.1:p.Tyr2695Ser
XM_011516852.1:c.8084A>C	XP_011515154.1:p.Tyr2695Ser
XM_011516854.1:c.6977A>C	XP_011515156.1:p.Tyr2326Ser
XM_005250800.3:c.11198A>C	XP_005250857.1:p.Tyr3733Ser
XM_005250801.5:c.11198A>C	XP_005250858.1:p.Tyr3733Ser
XM_011516848.2:c.11195A>C	XP_011515150.1:p.Tyr3732Ser
XM_011516849.2:c.11120A>C	XP_011515151.1:p.Tyr3707Ser
XM_011516850.2:c.10820A>C	XP_011515152.1:p.Tyr3607Ser
XM_011516851.2:c.8084A>C	XP_011515153.1:p.Tyr2695Ser
XM_011516852.2:c.8084A>C	XP_011515154.1:p.Tyr2695Ser
XM_011516854.2:c.6977A>C	XP_011515156.1:p.Tyr2326Ser
XM_017013109.1:c.11003A>C	XP_016868598.1:p.Tyr3668Ser
XM_017013111.1:c.8084A>C	XP_016868600.1:p.Tyr2695Ser
XM_017013112.1:c.6755A>C	XP_016868601.1:p.Tyr2252Ser
XM_024447074.1:c.9983A>C	XP_024302842.1:p.Tyr3328Ser
NM_017890.5:c.11198A>C MANE Plus Clinical	NP_060360.3:p.Tyr3733Ser
NM_152564.5:c.11123A>C MANE Select	NP_689777.3:p.Tyr3708Ser