Canonical Allele Identifier: CA1805814265

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99699155_99699156delinsTG , CM000670.2:g.99699155_99699156delinsTG	GRCh38
NC_000008.10:g.100711383_100711384delinsTG , CM000670.1:g.100711383_100711384delinsTG	GRCh37
NC_000008.9:g.100780559_100780560delinsTG	NCBI36
NG_007098.2:g.690890_690891delinsTG , LRG_351:g.690890_690891delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.6122-370_6122-369delinsTG	ENSP00000507923.1:n.6122-370_6122-369delinsTG
ENST00000682358.1:n.6192-370_6192-369delinsTG
ENST00000683334.1:c.*1804-370_*1804-369delinsTG	ENSP00000507369.1:n.*1804-370_*1804-369delinsTG
ENST00000357162.7:c.6047-370_6047-369delinsTG MANE Select	ENSP00000349685.2:n.6047-370_6047-369delinsTG
ENST00000358544.7:c.6122-370_6122-369delinsTG MANE Plus Clinical	ENSP00000351346.2:n.6122-370_6122-369delinsTG
ENST00000357162.6:c.6047-370_6047-369delinsTG	ENSP00000349685.2:n.6047-370_6047-369delinsTG
ENST00000358544.6:c.6122-370_6122-369delinsTG	ENSP00000351346.2:n.6122-370_6122-369delinsTG
NM_017890.4:c.6122-370_6122-369delinsTG , LRG_351t1:c.6122-370_6122-369delinsTG	NP_060360.3:n.6122-370_6122-369delinsTG
NM_152564.4:c.6047-370_6047-369delinsTG , LRG_351t2:c.6047-370_6047-369delinsTG	NP_689777.3:n.6047-370_6047-369delinsTG
XM_005250800.2:c.6122-370_6122-369delinsTG	XP_005250857.1:n.6122-370_6122-369delinsTG
XM_005250801.3:c.6122-370_6122-369delinsTG	XP_005250858.1:n.6122-370_6122-369delinsTG
XM_011516848.1:c.6119-370_6119-369delinsTG	XP_011515150.1:n.6119-370_6119-369delinsTG
XM_011516849.1:c.6044-370_6044-369delinsTG	XP_011515151.1:n.6044-370_6044-369delinsTG
XM_011516850.1:c.5744-370_5744-369delinsTG	XP_011515152.1:n.5744-370_5744-369delinsTG
XM_011516851.1:c.3008-370_3008-369delinsTG	XP_011515153.1:n.3008-370_3008-369delinsTG
XM_011516852.1:c.3008-370_3008-369delinsTG	XP_011515154.1:n.3008-370_3008-369delinsTG
XM_011516853.1:c.6122-370_6122-369delinsTG	XP_011515155.1:n.6122-370_6122-369delinsTG
XM_011516854.1:c.1901-370_1901-369delinsTG	XP_011515156.1:n.1901-370_1901-369delinsTG
XM_005250800.3:c.6122-370_6122-369delinsTG	XP_005250857.1:n.6122-370_6122-369delinsTG
XM_005250801.5:c.6122-370_6122-369delinsTG	XP_005250858.1:n.6122-370_6122-369delinsTG
XM_011516848.2:c.6119-370_6119-369delinsTG	XP_011515150.1:n.6119-370_6119-369delinsTG
XM_011516849.2:c.6044-370_6044-369delinsTG	XP_011515151.1:n.6044-370_6044-369delinsTG
XM_011516850.2:c.5744-370_5744-369delinsTG	XP_011515152.1:n.5744-370_5744-369delinsTG
XM_011516851.2:c.3008-370_3008-369delinsTG	XP_011515153.1:n.3008-370_3008-369delinsTG
XM_011516852.2:c.3008-370_3008-369delinsTG	XP_011515154.1:n.3008-370_3008-369delinsTG
XM_011516853.2:c.6122-370_6122-369delinsTG	XP_011515155.1:n.6122-370_6122-369delinsTG
XM_011516854.2:c.1901-370_1901-369delinsTG	XP_011515156.1:n.1901-370_1901-369delinsTG
XM_017013109.1:c.5927-370_5927-369delinsTG	XP_016868598.1:n.5927-370_5927-369delinsTG
XM_017013111.1:c.3008-370_3008-369delinsTG	XP_016868600.1:n.3008-370_3008-369delinsTG
XM_017013112.1:c.1679-370_1679-369delinsTG	XP_016868601.1:n.1679-370_1679-369delinsTG
XM_024447074.1:c.4907-370_4907-369delinsTG	XP_024302842.1:n.4907-370_4907-369delinsTG
XR_001745482.2:n.6083-370_6083-369delinsTG
NM_017890.5:c.6122-370_6122-369delinsTG MANE Plus Clinical	NP_060360.3:n.6122-370_6122-369delinsTG
NM_152564.5:c.6047-370_6047-369delinsTG MANE Select	NP_689777.3:n.6047-370_6047-369delinsTG