Canonical Allele Identifier: CA2781479915

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99835785_99835786insAC , CM000670.2:g.99835785_99835786insAC	GRCh38
NC_000008.10:g.100848013_100848014insAC , CM000670.1:g.100848013_100848014insAC	GRCh37
NC_000008.9:g.100917189_100917190insAC	NCBI36
NG_007098.2:g.827520_827521insAC , LRG_351:g.827520_827521insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.10017+47_10017+48insAC	ENSP00000507923.1:n.10017+47_10017+48insAC
ENST00000682358.1:n.10087+47_10087+48insAC
ENST00000683334.1:c.*5699+47_*5699+48insAC	ENSP00000507369.1:n.*5699+47_*5699+48insAC
ENST00000357162.7:c.9942+47_9942+48insAC MANE Select	ENSP00000349685.2:n.9942+47_9942+48insAC
ENST00000358544.7:c.10017+47_10017+48insAC MANE Plus Clinical	ENSP00000351346.2:n.10017+47_10017+48insAC
ENST00000357162.6:c.9942+47_9942+48insAC	ENSP00000349685.2:n.9942+47_9942+48insAC
ENST00000358544.6:c.10017+47_10017+48insAC	ENSP00000351346.2:n.10017+47_10017+48insAC
NM_017890.4:c.10017+47_10017+48insAC , LRG_351t1:c.10017+47_10017+48insAC	NP_060360.3:n.10017+47_10017+48insAC
NM_152564.4:c.9942+47_9942+48insAC , LRG_351t2:c.9942+47_9942+48insAC	NP_689777.3:n.9942+47_9942+48insAC
XM_005250800.2:c.10017+47_10017+48insAC	XP_005250857.1:n.10017+47_10017+48insAC
XM_005250801.3:c.10017+47_10017+48insAC	XP_005250858.1:n.10017+47_10017+48insAC
XM_011516848.1:c.10014+47_10014+48insAC	XP_011515150.1:n.10014+47_10014+48insAC
XM_011516849.1:c.9939+47_9939+48insAC	XP_011515151.1:n.9939+47_9939+48insAC
XM_011516850.1:c.9639+47_9639+48insAC	XP_011515152.1:n.9639+47_9639+48insAC
XM_011516851.1:c.6903+47_6903+48insAC	XP_011515153.1:n.6903+47_6903+48insAC
XM_011516852.1:c.6903+47_6903+48insAC	XP_011515154.1:n.6903+47_6903+48insAC
XM_011516854.1:c.5796+47_5796+48insAC	XP_011515156.1:n.5796+47_5796+48insAC
XM_005250800.3:c.10017+47_10017+48insAC	XP_005250857.1:n.10017+47_10017+48insAC
XM_005250801.5:c.10017+47_10017+48insAC	XP_005250858.1:n.10017+47_10017+48insAC
XM_011516848.2:c.10014+47_10014+48insAC	XP_011515150.1:n.10014+47_10014+48insAC
XM_011516849.2:c.9939+47_9939+48insAC	XP_011515151.1:n.9939+47_9939+48insAC
XM_011516850.2:c.9639+47_9639+48insAC	XP_011515152.1:n.9639+47_9639+48insAC
XM_011516851.2:c.6903+47_6903+48insAC	XP_011515153.1:n.6903+47_6903+48insAC
XM_011516852.2:c.6903+47_6903+48insAC	XP_011515154.1:n.6903+47_6903+48insAC
XM_011516854.2:c.5796+47_5796+48insAC	XP_011515156.1:n.5796+47_5796+48insAC
XM_017013109.1:c.9822+47_9822+48insAC	XP_016868598.1:n.9822+47_9822+48insAC
XM_017013111.1:c.6903+47_6903+48insAC	XP_016868600.1:n.6903+47_6903+48insAC
XM_017013112.1:c.5574+47_5574+48insAC	XP_016868601.1:n.5574+47_5574+48insAC
XM_024447074.1:c.8802+47_8802+48insAC	XP_024302842.1:n.8802+47_8802+48insAC
NM_017890.5:c.10017+47_10017+48insAC MANE Plus Clinical	NP_060360.3:n.10017+47_10017+48insAC
NM_152564.5:c.9942+47_9942+48insAC MANE Select	NP_689777.3:n.9942+47_9942+48insAC