Canonical Allele Identifier: CA2781476176

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99819699_99819700insA , CM000670.2:g.99819699_99819700insA	GRCh38
NC_000008.10:g.100831927_100831928insA , CM000670.1:g.100831927_100831928insA	GRCh37
NC_000008.9:g.100901103_100901104insA	NCBI36
NG_007098.2:g.811434_811435insA , LRG_351:g.811434_811435insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.8867+117_8867+118insA	ENSP00000507923.1:n.8867+117_8867+118insA
ENST00000682358.1:n.8937+117_8937+118insA
ENST00000683334.1:c.*4549+117_*4549+118insA	ENSP00000507369.1:n.*4549+117_*4549+118insA
ENST00000357162.7:c.8792+117_8792+118insA MANE Select	ENSP00000349685.2:n.8792+117_8792+118insA
ENST00000358544.7:c.8867+117_8867+118insA MANE Plus Clinical	ENSP00000351346.2:n.8867+117_8867+118insA
ENST00000357162.6:c.8792+117_8792+118insA	ENSP00000349685.2:n.8792+117_8792+118insA
ENST00000358544.6:c.8867+117_8867+118insA	ENSP00000351346.2:n.8867+117_8867+118insA
NM_017890.4:c.8867+117_8867+118insA , LRG_351t1:c.8867+117_8867+118insA	NP_060360.3:n.8867+117_8867+118insA
NM_152564.4:c.8792+117_8792+118insA , LRG_351t2:c.8792+117_8792+118insA	NP_689777.3:n.8792+117_8792+118insA
XM_005250800.2:c.8867+117_8867+118insA	XP_005250857.1:n.8867+117_8867+118insA
XM_005250801.3:c.8867+117_8867+118insA	XP_005250858.1:n.8867+117_8867+118insA
XM_011516848.1:c.8864+117_8864+118insA	XP_011515150.1:n.8864+117_8864+118insA
XM_011516849.1:c.8789+117_8789+118insA	XP_011515151.1:n.8789+117_8789+118insA
XM_011516850.1:c.8489+117_8489+118insA	XP_011515152.1:n.8489+117_8489+118insA
XM_011516851.1:c.5753+117_5753+118insA	XP_011515153.1:n.5753+117_5753+118insA
XM_011516852.1:c.5753+117_5753+118insA	XP_011515154.1:n.5753+117_5753+118insA
XM_011516854.1:c.4646+117_4646+118insA	XP_011515156.1:n.4646+117_4646+118insA
XM_005250800.3:c.8867+117_8867+118insA	XP_005250857.1:n.8867+117_8867+118insA
XM_005250801.5:c.8867+117_8867+118insA	XP_005250858.1:n.8867+117_8867+118insA
XM_011516848.2:c.8864+117_8864+118insA	XP_011515150.1:n.8864+117_8864+118insA
XM_011516849.2:c.8789+117_8789+118insA	XP_011515151.1:n.8789+117_8789+118insA
XM_011516850.2:c.8489+117_8489+118insA	XP_011515152.1:n.8489+117_8489+118insA
XM_011516851.2:c.5753+117_5753+118insA	XP_011515153.1:n.5753+117_5753+118insA
XM_011516852.2:c.5753+117_5753+118insA	XP_011515154.1:n.5753+117_5753+118insA
XM_011516854.2:c.4646+117_4646+118insA	XP_011515156.1:n.4646+117_4646+118insA
XM_017013109.1:c.8672+117_8672+118insA	XP_016868598.1:n.8672+117_8672+118insA
XM_017013111.1:c.5753+117_5753+118insA	XP_016868600.1:n.5753+117_5753+118insA
XM_017013112.1:c.4424+117_4424+118insA	XP_016868601.1:n.4424+117_4424+118insA
XM_024447074.1:c.7652+117_7652+118insA	XP_024302842.1:n.7652+117_7652+118insA
NM_017890.5:c.8867+117_8867+118insA MANE Plus Clinical	NP_060360.3:n.8867+117_8867+118insA
NM_152564.5:c.8792+117_8792+118insA MANE Select	NP_689777.3:n.8792+117_8792+118insA