Canonical Allele Identifier: CA371776763

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100831810G>C (hg19) ; chr8:g.99819582G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99819582G>C , CM000670.2:g.99819582G>C	GRCh38
NC_000008.10:g.100831810G>C , CM000670.1:g.100831810G>C	GRCh37
NC_000008.9:g.100900986G>C	NCBI36
NG_007098.2:g.811317G>C , LRG_351:g.811317G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.8867G>C	ENSP00000507923.1:p.Arg2956Thr
ENST00000682358.1:n.8937G>C
ENST00000683334.1:c.*4549G>C	ENSP00000507369.1:n.*4549G>C
ENST00000357162.7:c.8792G>C MANE Select	ENSP00000349685.2:p.Arg2931Thr
ENST00000358544.7:c.8867G>C MANE Plus Clinical	ENSP00000351346.2:p.Arg2956Thr
ENST00000357162.6:c.8792G>C	ENSP00000349685.2:p.Arg2931Thr
ENST00000358544.6:c.8867G>C	ENSP00000351346.2:p.Arg2956Thr
NM_017890.4:c.8867G>C , LRG_351t1:c.8867G>C	NP_060360.3:p.Arg2956Thr
NM_152564.4:c.8792G>C , LRG_351t2:c.8792G>C	NP_689777.3:p.Arg2931Thr
XM_005250800.2:c.8867G>C	XP_005250857.1:p.Arg2956Thr
XM_005250801.3:c.8867G>C	XP_005250858.1:p.Arg2956Thr
XM_011516848.1:c.8864G>C	XP_011515150.1:p.Arg2955Thr
XM_011516849.1:c.8789G>C	XP_011515151.1:p.Arg2930Thr
XM_011516850.1:c.8489G>C	XP_011515152.1:p.Arg2830Thr
XM_011516851.1:c.5753G>C	XP_011515153.1:p.Arg1918Thr
XM_011516852.1:c.5753G>C	XP_011515154.1:p.Arg1918Thr
XM_011516854.1:c.4646G>C	XP_011515156.1:p.Arg1549Thr
XM_005250800.3:c.8867G>C	XP_005250857.1:p.Arg2956Thr
XM_005250801.5:c.8867G>C	XP_005250858.1:p.Arg2956Thr
XM_011516848.2:c.8864G>C	XP_011515150.1:p.Arg2955Thr
XM_011516849.2:c.8789G>C	XP_011515151.1:p.Arg2930Thr
XM_011516850.2:c.8489G>C	XP_011515152.1:p.Arg2830Thr
XM_011516851.2:c.5753G>C	XP_011515153.1:p.Arg1918Thr
XM_011516852.2:c.5753G>C	XP_011515154.1:p.Arg1918Thr
XM_011516854.2:c.4646G>C	XP_011515156.1:p.Arg1549Thr
XM_017013109.1:c.8672G>C	XP_016868598.1:p.Arg2891Thr
XM_017013111.1:c.5753G>C	XP_016868600.1:p.Arg1918Thr
XM_017013112.1:c.4424G>C	XP_016868601.1:p.Arg1475Thr
XM_024447074.1:c.7652G>C	XP_024302842.1:p.Arg2551Thr
NM_017890.5:c.8867G>C MANE Plus Clinical	NP_060360.3:p.Arg2956Thr
NM_152564.5:c.8792G>C MANE Select	NP_689777.3:p.Arg2931Thr