Canonical Allele Identifier: CA1805814256

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99699153_99699156delinsTTTG , CM000670.2:g.99699153_99699156delinsTTTG	GRCh38
NC_000008.10:g.100711381_100711384delinsTTTG , CM000670.1:g.100711381_100711384delinsTTTG	GRCh37
NC_000008.9:g.100780557_100780560delinsTTTG	NCBI36
NG_007098.2:g.690888_690891delinsTTTG , LRG_351:g.690888_690891delinsTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.6122-372_6122-369delinsTTTG	ENSP00000507923.1:n.6122-372_6122-369delinsTTTG
ENST00000682358.1:n.6192-372_6192-369delinsTTTG
ENST00000683334.1:c.*1804-372_*1804-369delinsTTTG	ENSP00000507369.1:n.*1804-372_*1804-369delinsTTTG
ENST00000357162.7:c.6047-372_6047-369delinsTTTG MANE Select	ENSP00000349685.2:n.6047-372_6047-369delinsTTTG
ENST00000358544.7:c.6122-372_6122-369delinsTTTG MANE Plus Clinical	ENSP00000351346.2:n.6122-372_6122-369delinsTTTG
ENST00000357162.6:c.6047-372_6047-369delinsTTTG	ENSP00000349685.2:n.6047-372_6047-369delinsTTTG
ENST00000358544.6:c.6122-372_6122-369delinsTTTG	ENSP00000351346.2:n.6122-372_6122-369delinsTTTG
NM_017890.4:c.6122-372_6122-369delinsTTTG , LRG_351t1:c.6122-372_6122-369delinsTTTG	NP_060360.3:n.6122-372_6122-369delinsTTTG
NM_152564.4:c.6047-372_6047-369delinsTTTG , LRG_351t2:c.6047-372_6047-369delinsTTTG	NP_689777.3:n.6047-372_6047-369delinsTTTG
XM_005250800.2:c.6122-372_6122-369delinsTTTG	XP_005250857.1:n.6122-372_6122-369delinsTTTG
XM_005250801.3:c.6122-372_6122-369delinsTTTG	XP_005250858.1:n.6122-372_6122-369delinsTTTG
XM_011516848.1:c.6119-372_6119-369delinsTTTG	XP_011515150.1:n.6119-372_6119-369delinsTTTG
XM_011516849.1:c.6044-372_6044-369delinsTTTG	XP_011515151.1:n.6044-372_6044-369delinsTTTG
XM_011516850.1:c.5744-372_5744-369delinsTTTG	XP_011515152.1:n.5744-372_5744-369delinsTTTG
XM_011516851.1:c.3008-372_3008-369delinsTTTG	XP_011515153.1:n.3008-372_3008-369delinsTTTG
XM_011516852.1:c.3008-372_3008-369delinsTTTG	XP_011515154.1:n.3008-372_3008-369delinsTTTG
XM_011516853.1:c.6122-372_6122-369delinsTTTG	XP_011515155.1:n.6122-372_6122-369delinsTTTG
XM_011516854.1:c.1901-372_1901-369delinsTTTG	XP_011515156.1:n.1901-372_1901-369delinsTTTG
XM_005250800.3:c.6122-372_6122-369delinsTTTG	XP_005250857.1:n.6122-372_6122-369delinsTTTG
XM_005250801.5:c.6122-372_6122-369delinsTTTG	XP_005250858.1:n.6122-372_6122-369delinsTTTG
XM_011516848.2:c.6119-372_6119-369delinsTTTG	XP_011515150.1:n.6119-372_6119-369delinsTTTG
XM_011516849.2:c.6044-372_6044-369delinsTTTG	XP_011515151.1:n.6044-372_6044-369delinsTTTG
XM_011516850.2:c.5744-372_5744-369delinsTTTG	XP_011515152.1:n.5744-372_5744-369delinsTTTG
XM_011516851.2:c.3008-372_3008-369delinsTTTG	XP_011515153.1:n.3008-372_3008-369delinsTTTG
XM_011516852.2:c.3008-372_3008-369delinsTTTG	XP_011515154.1:n.3008-372_3008-369delinsTTTG
XM_011516853.2:c.6122-372_6122-369delinsTTTG	XP_011515155.1:n.6122-372_6122-369delinsTTTG
XM_011516854.2:c.1901-372_1901-369delinsTTTG	XP_011515156.1:n.1901-372_1901-369delinsTTTG
XM_017013109.1:c.5927-372_5927-369delinsTTTG	XP_016868598.1:n.5927-372_5927-369delinsTTTG
XM_017013111.1:c.3008-372_3008-369delinsTTTG	XP_016868600.1:n.3008-372_3008-369delinsTTTG
XM_017013112.1:c.1679-372_1679-369delinsTTTG	XP_016868601.1:n.1679-372_1679-369delinsTTTG
XM_024447074.1:c.4907-372_4907-369delinsTTTG	XP_024302842.1:n.4907-372_4907-369delinsTTTG
XR_001745482.2:n.6083-372_6083-369delinsTTTG
NM_017890.5:c.6122-372_6122-369delinsTTTG MANE Plus Clinical	NP_060360.3:n.6122-372_6122-369delinsTTTG
NM_152564.5:c.6047-372_6047-369delinsTTTG MANE Select	NP_689777.3:n.6047-372_6047-369delinsTTTG