Canonical Allele Identifier: CA2781479986

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99835853_99835857del , CM000670.2:g.99835853_99835857del	GRCh38
NC_000008.10:g.100848081_100848085del , CM000670.1:g.100848081_100848085del	GRCh37
NC_000008.9:g.100917257_100917261del	NCBI36
NG_007098.2:g.827588_827592del , LRG_351:g.827588_827592del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.10017+115_10017+119del	ENSP00000507923.1:n.10017+115_10017+119del
ENST00000682358.1:n.10087+115_10087+119del
ENST00000683334.1:c.*5699+115_*5699+119del	ENSP00000507369.1:n.*5699+115_*5699+119del
ENST00000357162.7:c.9942+115_9942+119del MANE Select	ENSP00000349685.2:n.9942+115_9942+119del
ENST00000358544.7:c.10017+115_10017+119del MANE Plus Clinical	ENSP00000351346.2:n.10017+115_10017+119del
ENST00000357162.6:c.9942+115_9942+119del	ENSP00000349685.2:n.9942+115_9942+119del
ENST00000358544.6:c.10017+115_10017+119del	ENSP00000351346.2:n.10017+115_10017+119del
NM_017890.4:c.10017+115_10017+119del , LRG_351t1:c.10017+115_10017+119del	NP_060360.3:n.10017+115_10017+119del
NM_152564.4:c.9942+115_9942+119del , LRG_351t2:c.9942+115_9942+119del	NP_689777.3:n.9942+115_9942+119del
XM_005250800.2:c.10017+115_10017+119del	XP_005250857.1:n.10017+115_10017+119del
XM_005250801.3:c.10017+115_10017+119del	XP_005250858.1:n.10017+115_10017+119del
XM_011516848.1:c.10014+115_10014+119del	XP_011515150.1:n.10014+115_10014+119del
XM_011516849.1:c.9939+115_9939+119del	XP_011515151.1:n.9939+115_9939+119del
XM_011516850.1:c.9639+115_9639+119del	XP_011515152.1:n.9639+115_9639+119del
XM_011516851.1:c.6903+115_6903+119del	XP_011515153.1:n.6903+115_6903+119del
XM_011516852.1:c.6903+115_6903+119del	XP_011515154.1:n.6903+115_6903+119del
XM_011516854.1:c.5796+115_5796+119del	XP_011515156.1:n.5796+115_5796+119del
XM_005250800.3:c.10017+115_10017+119del	XP_005250857.1:n.10017+115_10017+119del
XM_005250801.5:c.10017+115_10017+119del	XP_005250858.1:n.10017+115_10017+119del
XM_011516848.2:c.10014+115_10014+119del	XP_011515150.1:n.10014+115_10014+119del
XM_011516849.2:c.9939+115_9939+119del	XP_011515151.1:n.9939+115_9939+119del
XM_011516850.2:c.9639+115_9639+119del	XP_011515152.1:n.9639+115_9639+119del
XM_011516851.2:c.6903+115_6903+119del	XP_011515153.1:n.6903+115_6903+119del
XM_011516852.2:c.6903+115_6903+119del	XP_011515154.1:n.6903+115_6903+119del
XM_011516854.2:c.5796+115_5796+119del	XP_011515156.1:n.5796+115_5796+119del
XM_017013109.1:c.9822+115_9822+119del	XP_016868598.1:n.9822+115_9822+119del
XM_017013111.1:c.6903+115_6903+119del	XP_016868600.1:n.6903+115_6903+119del
XM_017013112.1:c.5574+115_5574+119del	XP_016868601.1:n.5574+115_5574+119del
XM_024447074.1:c.8802+115_8802+119del	XP_024302842.1:n.8802+115_8802+119del
NM_017890.5:c.10017+115_10017+119del MANE Plus Clinical	NP_060360.3:n.10017+115_10017+119del
NM_152564.5:c.9942+115_9942+119del MANE Select	NP_689777.3:n.9942+115_9942+119del