Canonical Allele Identifier: CA371792054

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100880602G>T (hg19) ; chr8:g.99868374G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868374G>T , CM000670.2:g.99868374G>T	GRCh38
NC_000008.10:g.100880602G>T , CM000670.1:g.100880602G>T	GRCh37
NC_000008.9:g.100949778G>T	NCBI36
NG_007098.2:g.860109G>T , LRG_351:g.860109G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*470G>T	ENSP00000507923.1:n.*470G>T
ENST00000682358.1:n.11446G>T
ENST00000683334.1:c.*7058G>T	ENSP00000507369.1:n.*7058G>T
ENST00000357162.7:c.11301G>T MANE Select	ENSP00000349685.2:p.Lys3767Asn
ENST00000358544.7:c.11376G>T MANE Plus Clinical	ENSP00000351346.2:p.Lys3792Asn
ENST00000357162.6:c.11301G>T	ENSP00000349685.2:p.Lys3767Asn
ENST00000358544.6:c.11376G>T	ENSP00000351346.2:p.Lys3792Asn
ENST00000493587.1:n.318G>T
NM_017890.4:c.11376G>T , LRG_351t1:c.11376G>T	NP_060360.3:p.Lys3792Asn
NM_152564.4:c.11301G>T , LRG_351t2:c.11301G>T	NP_689777.3:p.Lys3767Asn
XM_005250800.2:c.11376G>T	XP_005250857.1:p.Lys3792Asn
XM_005250801.3:c.11376G>T	XP_005250858.1:p.Lys3792Asn
XM_011516848.1:c.11373G>T	XP_011515150.1:p.Lys3791Asn
XM_011516849.1:c.11298G>T	XP_011515151.1:p.Lys3766Asn
XM_011516850.1:c.10998G>T	XP_011515152.1:p.Lys3666Asn
XM_011516851.1:c.8262G>T	XP_011515153.1:p.Lys2754Asn
XM_011516852.1:c.8262G>T	XP_011515154.1:p.Lys2754Asn
XM_011516854.1:c.7155G>T	XP_011515156.1:p.Lys2385Asn
XM_005250800.3:c.11376G>T	XP_005250857.1:p.Lys3792Asn
XM_005250801.5:c.11376G>T	XP_005250858.1:p.Lys3792Asn
XM_011516848.2:c.11373G>T	XP_011515150.1:p.Lys3791Asn
XM_011516849.2:c.11298G>T	XP_011515151.1:p.Lys3766Asn
XM_011516850.2:c.10998G>T	XP_011515152.1:p.Lys3666Asn
XM_011516851.2:c.8262G>T	XP_011515153.1:p.Lys2754Asn
XM_011516852.2:c.8262G>T	XP_011515154.1:p.Lys2754Asn
XM_011516854.2:c.7155G>T	XP_011515156.1:p.Lys2385Asn
XM_017013109.1:c.11181G>T	XP_016868598.1:p.Lys3727Asn
XM_017013111.1:c.8262G>T	XP_016868600.1:p.Lys2754Asn
XM_017013112.1:c.6933G>T	XP_016868601.1:p.Lys2311Asn
XM_024447074.1:c.10161G>T	XP_024302842.1:p.Lys3387Asn
NM_017890.5:c.11376G>T MANE Plus Clinical	NP_060360.3:p.Lys3792Asn
NM_152564.5:c.11301G>T MANE Select	NP_689777.3:p.Lys3767Asn