Canonical Allele Identifier: CA371784970

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100847947T>C (hg19) ; chr8:g.99835719T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99835719T>C , CM000670.2:g.99835719T>C	GRCh38
NC_000008.10:g.100847947T>C , CM000670.1:g.100847947T>C	GRCh37
NC_000008.9:g.100917123T>C	NCBI36
NG_007098.2:g.827454T>C , LRG_351:g.827454T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.9998T>C	ENSP00000507923.1:p.Ile3333Thr
ENST00000682358.1:n.10068T>C
ENST00000683334.1:c.*5680T>C	ENSP00000507369.1:n.*5680T>C
ENST00000357162.7:c.9923T>C MANE Select	ENSP00000349685.2:p.Ile3308Thr
ENST00000358544.7:c.9998T>C MANE Plus Clinical	ENSP00000351346.2:p.Ile3333Thr
ENST00000357162.6:c.9923T>C	ENSP00000349685.2:p.Ile3308Thr
ENST00000358544.6:c.9998T>C	ENSP00000351346.2:p.Ile3333Thr
NM_017890.4:c.9998T>C , LRG_351t1:c.9998T>C	NP_060360.3:p.Ile3333Thr
NM_152564.4:c.9923T>C , LRG_351t2:c.9923T>C	NP_689777.3:p.Ile3308Thr
XM_005250800.2:c.9998T>C	XP_005250857.1:p.Ile3333Thr
XM_005250801.3:c.9998T>C	XP_005250858.1:p.Ile3333Thr
XM_011516848.1:c.9995T>C	XP_011515150.1:p.Ile3332Thr
XM_011516849.1:c.9920T>C	XP_011515151.1:p.Ile3307Thr
XM_011516850.1:c.9620T>C	XP_011515152.1:p.Ile3207Thr
XM_011516851.1:c.6884T>C	XP_011515153.1:p.Ile2295Thr
XM_011516852.1:c.6884T>C	XP_011515154.1:p.Ile2295Thr
XM_011516854.1:c.5777T>C	XP_011515156.1:p.Ile1926Thr
XM_005250800.3:c.9998T>C	XP_005250857.1:p.Ile3333Thr
XM_005250801.5:c.9998T>C	XP_005250858.1:p.Ile3333Thr
XM_011516848.2:c.9995T>C	XP_011515150.1:p.Ile3332Thr
XM_011516849.2:c.9920T>C	XP_011515151.1:p.Ile3307Thr
XM_011516850.2:c.9620T>C	XP_011515152.1:p.Ile3207Thr
XM_011516851.2:c.6884T>C	XP_011515153.1:p.Ile2295Thr
XM_011516852.2:c.6884T>C	XP_011515154.1:p.Ile2295Thr
XM_011516854.2:c.5777T>C	XP_011515156.1:p.Ile1926Thr
XM_017013109.1:c.9803T>C	XP_016868598.1:p.Ile3268Thr
XM_017013111.1:c.6884T>C	XP_016868600.1:p.Ile2295Thr
XM_017013112.1:c.5555T>C	XP_016868601.1:p.Ile1852Thr
XM_024447074.1:c.8783T>C	XP_024302842.1:p.Ile2928Thr
NM_017890.5:c.9998T>C MANE Plus Clinical	NP_060360.3:p.Ile3333Thr
NM_152564.5:c.9923T>C MANE Select	NP_689777.3:p.Ile3308Thr