Canonical Allele Identifier: CA1805814083

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99699129_99699135delinsGTCTTTT , CM000670.2:g.99699129_99699135delinsGTCTTTT	GRCh38
NC_000008.10:g.100711357_100711363delinsGTCTTTT , CM000670.1:g.100711357_100711363delinsGTCTTTT	GRCh37
NC_000008.9:g.100780533_100780539delinsGTCTTTT	NCBI36
NG_007098.2:g.690864_690870delinsGTCTTTT , LRG_351:g.690864_690870delinsGTCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.6122-396_6122-390delinsGTCTTTT	ENSP00000507923.1:n.6122-396_6122-390delinsGTCTTTT
ENST00000682358.1:n.6192-396_6192-390delinsGTCTTTT
ENST00000683334.1:c.*1804-396_*1804-390delinsGTCTTTT	ENSP00000507369.1:n.*1804-396_*1804-390delinsGTCTTTT
ENST00000357162.7:c.6047-396_6047-390delinsGTCTTTT MANE Select	ENSP00000349685.2:n.6047-396_6047-390delinsGTCTTTT
ENST00000358544.7:c.6122-396_6122-390delinsGTCTTTT MANE Plus Clinical	ENSP00000351346.2:n.6122-396_6122-390delinsGTCTTTT
ENST00000357162.6:c.6047-396_6047-390delinsGTCTTTT	ENSP00000349685.2:n.6047-396_6047-390delinsGTCTTTT
ENST00000358544.6:c.6122-396_6122-390delinsGTCTTTT	ENSP00000351346.2:n.6122-396_6122-390delinsGTCTTTT
NM_017890.4:c.6122-396_6122-390delinsGTCTTTT , LRG_351t1:c.6122-396_6122-390delinsGTCTTTT	NP_060360.3:n.6122-396_6122-390delinsGTCTTTT
NM_152564.4:c.6047-396_6047-390delinsGTCTTTT , LRG_351t2:c.6047-396_6047-390delinsGTCTTTT	NP_689777.3:n.6047-396_6047-390delinsGTCTTTT
XM_005250800.2:c.6122-396_6122-390delinsGTCTTTT	XP_005250857.1:n.6122-396_6122-390delinsGTCTTTT
XM_005250801.3:c.6122-396_6122-390delinsGTCTTTT	XP_005250858.1:n.6122-396_6122-390delinsGTCTTTT
XM_011516848.1:c.6119-396_6119-390delinsGTCTTTT	XP_011515150.1:n.6119-396_6119-390delinsGTCTTTT
XM_011516849.1:c.6044-396_6044-390delinsGTCTTTT	XP_011515151.1:n.6044-396_6044-390delinsGTCTTTT
XM_011516850.1:c.5744-396_5744-390delinsGTCTTTT	XP_011515152.1:n.5744-396_5744-390delinsGTCTTTT
XM_011516851.1:c.3008-396_3008-390delinsGTCTTTT	XP_011515153.1:n.3008-396_3008-390delinsGTCTTTT
XM_011516852.1:c.3008-396_3008-390delinsGTCTTTT	XP_011515154.1:n.3008-396_3008-390delinsGTCTTTT
XM_011516853.1:c.6122-396_6122-390delinsGTCTTTT	XP_011515155.1:n.6122-396_6122-390delinsGTCTTTT
XM_011516854.1:c.1901-396_1901-390delinsGTCTTTT	XP_011515156.1:n.1901-396_1901-390delinsGTCTTTT
XM_005250800.3:c.6122-396_6122-390delinsGTCTTTT	XP_005250857.1:n.6122-396_6122-390delinsGTCTTTT
XM_005250801.5:c.6122-396_6122-390delinsGTCTTTT	XP_005250858.1:n.6122-396_6122-390delinsGTCTTTT
XM_011516848.2:c.6119-396_6119-390delinsGTCTTTT	XP_011515150.1:n.6119-396_6119-390delinsGTCTTTT
XM_011516849.2:c.6044-396_6044-390delinsGTCTTTT	XP_011515151.1:n.6044-396_6044-390delinsGTCTTTT
XM_011516850.2:c.5744-396_5744-390delinsGTCTTTT	XP_011515152.1:n.5744-396_5744-390delinsGTCTTTT
XM_011516851.2:c.3008-396_3008-390delinsGTCTTTT	XP_011515153.1:n.3008-396_3008-390delinsGTCTTTT
XM_011516852.2:c.3008-396_3008-390delinsGTCTTTT	XP_011515154.1:n.3008-396_3008-390delinsGTCTTTT
XM_011516853.2:c.6122-396_6122-390delinsGTCTTTT	XP_011515155.1:n.6122-396_6122-390delinsGTCTTTT
XM_011516854.2:c.1901-396_1901-390delinsGTCTTTT	XP_011515156.1:n.1901-396_1901-390delinsGTCTTTT
XM_017013109.1:c.5927-396_5927-390delinsGTCTTTT	XP_016868598.1:n.5927-396_5927-390delinsGTCTTTT
XM_017013111.1:c.3008-396_3008-390delinsGTCTTTT	XP_016868600.1:n.3008-396_3008-390delinsGTCTTTT
XM_017013112.1:c.1679-396_1679-390delinsGTCTTTT	XP_016868601.1:n.1679-396_1679-390delinsGTCTTTT
XM_024447074.1:c.4907-396_4907-390delinsGTCTTTT	XP_024302842.1:n.4907-396_4907-390delinsGTCTTTT
XR_001745482.2:n.6083-396_6083-390delinsGTCTTTT
NM_017890.5:c.6122-396_6122-390delinsGTCTTTT MANE Plus Clinical	NP_060360.3:n.6122-396_6122-390delinsGTCTTTT
NM_152564.5:c.6047-396_6047-390delinsGTCTTTT MANE Select	NP_689777.3:n.6047-396_6047-390delinsGTCTTTT