Canonical Allele Identifier: CA2781479983

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99835848_99835860del , CM000670.2:g.99835848_99835860del	GRCh38
NC_000008.10:g.100848076_100848088del , CM000670.1:g.100848076_100848088del	GRCh37
NC_000008.9:g.100917252_100917264del	NCBI36
NG_007098.2:g.827583_827595del , LRG_351:g.827583_827595del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.10017+110_10017+122del	ENSP00000507923.1:n.10017+110_10017+122del
ENST00000682358.1:n.10087+110_10087+122del
ENST00000683334.1:c.*5699+110_*5699+122del	ENSP00000507369.1:n.*5699+110_*5699+122del
ENST00000357162.7:c.9942+110_9942+122del MANE Select	ENSP00000349685.2:n.9942+110_9942+122del
ENST00000358544.7:c.10017+110_10017+122del MANE Plus Clinical	ENSP00000351346.2:n.10017+110_10017+122del
ENST00000357162.6:c.9942+110_9942+122del	ENSP00000349685.2:n.9942+110_9942+122del
ENST00000358544.6:c.10017+110_10017+122del	ENSP00000351346.2:n.10017+110_10017+122del
NM_017890.4:c.10017+110_10017+122del , LRG_351t1:c.10017+110_10017+122del	NP_060360.3:n.10017+110_10017+122del
NM_152564.4:c.9942+110_9942+122del , LRG_351t2:c.9942+110_9942+122del	NP_689777.3:n.9942+110_9942+122del
XM_005250800.2:c.10017+110_10017+122del	XP_005250857.1:n.10017+110_10017+122del
XM_005250801.3:c.10017+110_10017+122del	XP_005250858.1:n.10017+110_10017+122del
XM_011516848.1:c.10014+110_10014+122del	XP_011515150.1:n.10014+110_10014+122del
XM_011516849.1:c.9939+110_9939+122del	XP_011515151.1:n.9939+110_9939+122del
XM_011516850.1:c.9639+110_9639+122del	XP_011515152.1:n.9639+110_9639+122del
XM_011516851.1:c.6903+110_6903+122del	XP_011515153.1:n.6903+110_6903+122del
XM_011516852.1:c.6903+110_6903+122del	XP_011515154.1:n.6903+110_6903+122del
XM_011516854.1:c.5796+110_5796+122del	XP_011515156.1:n.5796+110_5796+122del
XM_005250800.3:c.10017+110_10017+122del	XP_005250857.1:n.10017+110_10017+122del
XM_005250801.5:c.10017+110_10017+122del	XP_005250858.1:n.10017+110_10017+122del
XM_011516848.2:c.10014+110_10014+122del	XP_011515150.1:n.10014+110_10014+122del
XM_011516849.2:c.9939+110_9939+122del	XP_011515151.1:n.9939+110_9939+122del
XM_011516850.2:c.9639+110_9639+122del	XP_011515152.1:n.9639+110_9639+122del
XM_011516851.2:c.6903+110_6903+122del	XP_011515153.1:n.6903+110_6903+122del
XM_011516852.2:c.6903+110_6903+122del	XP_011515154.1:n.6903+110_6903+122del
XM_011516854.2:c.5796+110_5796+122del	XP_011515156.1:n.5796+110_5796+122del
XM_017013109.1:c.9822+110_9822+122del	XP_016868598.1:n.9822+110_9822+122del
XM_017013111.1:c.6903+110_6903+122del	XP_016868600.1:n.6903+110_6903+122del
XM_017013112.1:c.5574+110_5574+122del	XP_016868601.1:n.5574+110_5574+122del
XM_024447074.1:c.8802+110_8802+122del	XP_024302842.1:n.8802+110_8802+122del
NM_017890.5:c.10017+110_10017+122del MANE Plus Clinical	NP_060360.3:n.10017+110_10017+122del
NM_152564.5:c.9942+110_9942+122del MANE Select	NP_689777.3:n.9942+110_9942+122del