Canonical Allele Identifier: CA1805814103

Gene: VPS13B

Linked Data

• dbSNP Id: rs1832161185

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99699130_99699131insA , CM000670.2:g.99699130_99699131insA	GRCh38
NC_000008.10:g.100711358_100711359insA , CM000670.1:g.100711358_100711359insA	GRCh37
NC_000008.9:g.100780534_100780535insA	NCBI36
NG_007098.2:g.690865_690866insA , LRG_351:g.690865_690866insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.6122-395_6122-394insA	ENSP00000507923.1:n.6122-395_6122-394insA
ENST00000682358.1:n.6192-395_6192-394insA
ENST00000683334.1:c.*1804-395_*1804-394insA	ENSP00000507369.1:n.*1804-395_*1804-394insA
ENST00000357162.7:c.6047-395_6047-394insA MANE Select	ENSP00000349685.2:n.6047-395_6047-394insA
ENST00000358544.7:c.6122-395_6122-394insA MANE Plus Clinical	ENSP00000351346.2:n.6122-395_6122-394insA
ENST00000357162.6:c.6047-395_6047-394insA	ENSP00000349685.2:n.6047-395_6047-394insA
ENST00000358544.6:c.6122-395_6122-394insA	ENSP00000351346.2:n.6122-395_6122-394insA
NM_017890.4:c.6122-395_6122-394insA , LRG_351t1:c.6122-395_6122-394insA	NP_060360.3:n.6122-395_6122-394insA
NM_152564.4:c.6047-395_6047-394insA , LRG_351t2:c.6047-395_6047-394insA	NP_689777.3:n.6047-395_6047-394insA
XM_005250800.2:c.6122-395_6122-394insA	XP_005250857.1:n.6122-395_6122-394insA
XM_005250801.3:c.6122-395_6122-394insA	XP_005250858.1:n.6122-395_6122-394insA
XM_011516848.1:c.6119-395_6119-394insA	XP_011515150.1:n.6119-395_6119-394insA
XM_011516849.1:c.6044-395_6044-394insA	XP_011515151.1:n.6044-395_6044-394insA
XM_011516850.1:c.5744-395_5744-394insA	XP_011515152.1:n.5744-395_5744-394insA
XM_011516851.1:c.3008-395_3008-394insA	XP_011515153.1:n.3008-395_3008-394insA
XM_011516852.1:c.3008-395_3008-394insA	XP_011515154.1:n.3008-395_3008-394insA
XM_011516853.1:c.6122-395_6122-394insA	XP_011515155.1:n.6122-395_6122-394insA
XM_011516854.1:c.1901-395_1901-394insA	XP_011515156.1:n.1901-395_1901-394insA
XM_005250800.3:c.6122-395_6122-394insA	XP_005250857.1:n.6122-395_6122-394insA
XM_005250801.5:c.6122-395_6122-394insA	XP_005250858.1:n.6122-395_6122-394insA
XM_011516848.2:c.6119-395_6119-394insA	XP_011515150.1:n.6119-395_6119-394insA
XM_011516849.2:c.6044-395_6044-394insA	XP_011515151.1:n.6044-395_6044-394insA
XM_011516850.2:c.5744-395_5744-394insA	XP_011515152.1:n.5744-395_5744-394insA
XM_011516851.2:c.3008-395_3008-394insA	XP_011515153.1:n.3008-395_3008-394insA
XM_011516852.2:c.3008-395_3008-394insA	XP_011515154.1:n.3008-395_3008-394insA
XM_011516853.2:c.6122-395_6122-394insA	XP_011515155.1:n.6122-395_6122-394insA
XM_011516854.2:c.1901-395_1901-394insA	XP_011515156.1:n.1901-395_1901-394insA
XM_017013109.1:c.5927-395_5927-394insA	XP_016868598.1:n.5927-395_5927-394insA
XM_017013111.1:c.3008-395_3008-394insA	XP_016868600.1:n.3008-395_3008-394insA
XM_017013112.1:c.1679-395_1679-394insA	XP_016868601.1:n.1679-395_1679-394insA
XM_024447074.1:c.4907-395_4907-394insA	XP_024302842.1:n.4907-395_4907-394insA
XR_001745482.2:n.6083-395_6083-394insA
NM_017890.5:c.6122-395_6122-394insA MANE Plus Clinical	NP_060360.3:n.6122-395_6122-394insA
NM_152564.5:c.6047-395_6047-394insA MANE Select	NP_689777.3:n.6047-395_6047-394insA