Canonical Allele Identifier: CA2781476814

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99717496_99717509del , CM000670.2:g.99717496_99717509del	GRCh38
NC_000008.10:g.100729724_100729737del , CM000670.1:g.100729724_100729737del	GRCh37
NC_000008.9:g.100798900_100798913del	NCBI36
NG_007098.2:g.709231_709244del , LRG_351:g.709231_709244del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.6732+123_6732+136del	ENSP00000507923.1:n.6732+123_6732+136del
ENST00000682358.1:n.6802+123_6802+136del
ENST00000683334.1:c.*2414+123_*2414+136del	ENSP00000507369.1:n.*2414+123_*2414+136del
ENST00000357162.7:c.6657+123_6657+136del MANE Select	ENSP00000349685.2:n.6657+123_6657+136del
ENST00000358544.7:c.6732+123_6732+136del MANE Plus Clinical	ENSP00000351346.2:n.6732+123_6732+136del
ENST00000357162.6:c.6657+123_6657+136del	ENSP00000349685.2:n.6657+123_6657+136del
ENST00000358544.6:c.6732+123_6732+136del	ENSP00000351346.2:n.6732+123_6732+136del
NM_017890.4:c.6732+123_6732+136del , LRG_351t1:c.6732+123_6732+136del	NP_060360.3:n.6732+123_6732+136del
NM_152564.4:c.6657+123_6657+136del , LRG_351t2:c.6657+123_6657+136del	NP_689777.3:n.6657+123_6657+136del
XM_005250800.2:c.6732+123_6732+136del	XP_005250857.1:n.6732+123_6732+136del
XM_005250801.3:c.6732+123_6732+136del	XP_005250858.1:n.6732+123_6732+136del
XM_011516848.1:c.6729+123_6729+136del	XP_011515150.1:n.6729+123_6729+136del
XM_011516849.1:c.6654+123_6654+136del	XP_011515151.1:n.6654+123_6654+136del
XM_011516850.1:c.6354+123_6354+136del	XP_011515152.1:n.6354+123_6354+136del
XM_011516851.1:c.3618+123_3618+136del	XP_011515153.1:n.3618+123_3618+136del
XM_011516852.1:c.3618+123_3618+136del	XP_011515154.1:n.3618+123_3618+136del
XM_011516853.1:c.6732+123_6732+136del	XP_011515155.1:n.6732+123_6732+136del
XM_011516854.1:c.2511+123_2511+136del	XP_011515156.1:n.2511+123_2511+136del
XM_005250800.3:c.6732+123_6732+136del	XP_005250857.1:n.6732+123_6732+136del
XM_005250801.5:c.6732+123_6732+136del	XP_005250858.1:n.6732+123_6732+136del
XM_011516848.2:c.6729+123_6729+136del	XP_011515150.1:n.6729+123_6729+136del
XM_011516849.2:c.6654+123_6654+136del	XP_011515151.1:n.6654+123_6654+136del
XM_011516850.2:c.6354+123_6354+136del	XP_011515152.1:n.6354+123_6354+136del
XM_011516851.2:c.3618+123_3618+136del	XP_011515153.1:n.3618+123_3618+136del
XM_011516852.2:c.3618+123_3618+136del	XP_011515154.1:n.3618+123_3618+136del
XM_011516853.2:c.6732+123_6732+136del	XP_011515155.1:n.6732+123_6732+136del
XM_011516854.2:c.2511+123_2511+136del	XP_011515156.1:n.2511+123_2511+136del
XM_017013109.1:c.6537+123_6537+136del	XP_016868598.1:n.6537+123_6537+136del
XM_017013111.1:c.3618+123_3618+136del	XP_016868600.1:n.3618+123_3618+136del
XM_017013112.1:c.2289+123_2289+136del	XP_016868601.1:n.2289+123_2289+136del
XM_024447074.1:c.5517+123_5517+136del	XP_024302842.1:n.5517+123_5517+136del
NM_017890.5:c.6732+123_6732+136del MANE Plus Clinical	NP_060360.3:n.6732+123_6732+136del
NM_152564.5:c.6657+123_6657+136del MANE Select	NP_689777.3:n.6657+123_6657+136del