Canonical Allele Identifier: CA2781476184

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99819731_99819732insACA , CM000670.2:g.99819731_99819732insACA	GRCh38
NC_000008.10:g.100831959_100831960insACA , CM000670.1:g.100831959_100831960insACA	GRCh37
NC_000008.9:g.100901135_100901136insACA	NCBI36
NG_007098.2:g.811466_811467insACA , LRG_351:g.811466_811467insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.8867+149_8867+150insACA	ENSP00000507923.1:n.8867+149_8867+150insACA
ENST00000682358.1:n.8937+149_8937+150insACA
ENST00000683334.1:c.*4549+149_*4549+150insACA	ENSP00000507369.1:n.*4549+149_*4549+150insACA
ENST00000357162.7:c.8792+149_8792+150insACA MANE Select	ENSP00000349685.2:n.8792+149_8792+150insACA
ENST00000358544.7:c.8867+149_8867+150insACA MANE Plus Clinical	ENSP00000351346.2:n.8867+149_8867+150insACA
ENST00000357162.6:c.8792+149_8792+150insACA	ENSP00000349685.2:n.8792+149_8792+150insACA
ENST00000358544.6:c.8867+149_8867+150insACA	ENSP00000351346.2:n.8867+149_8867+150insACA
NM_017890.4:c.8867+149_8867+150insACA , LRG_351t1:c.8867+149_8867+150insACA	NP_060360.3:n.8867+149_8867+150insACA
NM_152564.4:c.8792+149_8792+150insACA , LRG_351t2:c.8792+149_8792+150insACA	NP_689777.3:n.8792+149_8792+150insACA
XM_005250800.2:c.8867+149_8867+150insACA	XP_005250857.1:n.8867+149_8867+150insACA
XM_005250801.3:c.8867+149_8867+150insACA	XP_005250858.1:n.8867+149_8867+150insACA
XM_011516848.1:c.8864+149_8864+150insACA	XP_011515150.1:n.8864+149_8864+150insACA
XM_011516849.1:c.8789+149_8789+150insACA	XP_011515151.1:n.8789+149_8789+150insACA
XM_011516850.1:c.8489+149_8489+150insACA	XP_011515152.1:n.8489+149_8489+150insACA
XM_011516851.1:c.5753+149_5753+150insACA	XP_011515153.1:n.5753+149_5753+150insACA
XM_011516852.1:c.5753+149_5753+150insACA	XP_011515154.1:n.5753+149_5753+150insACA
XM_011516854.1:c.4646+149_4646+150insACA	XP_011515156.1:n.4646+149_4646+150insACA
XM_005250800.3:c.8867+149_8867+150insACA	XP_005250857.1:n.8867+149_8867+150insACA
XM_005250801.5:c.8867+149_8867+150insACA	XP_005250858.1:n.8867+149_8867+150insACA
XM_011516848.2:c.8864+149_8864+150insACA	XP_011515150.1:n.8864+149_8864+150insACA
XM_011516849.2:c.8789+149_8789+150insACA	XP_011515151.1:n.8789+149_8789+150insACA
XM_011516850.2:c.8489+149_8489+150insACA	XP_011515152.1:n.8489+149_8489+150insACA
XM_011516851.2:c.5753+149_5753+150insACA	XP_011515153.1:n.5753+149_5753+150insACA
XM_011516852.2:c.5753+149_5753+150insACA	XP_011515154.1:n.5753+149_5753+150insACA
XM_011516854.2:c.4646+149_4646+150insACA	XP_011515156.1:n.4646+149_4646+150insACA
XM_017013109.1:c.8672+149_8672+150insACA	XP_016868598.1:n.8672+149_8672+150insACA
XM_017013111.1:c.5753+149_5753+150insACA	XP_016868600.1:n.5753+149_5753+150insACA
XM_017013112.1:c.4424+149_4424+150insACA	XP_016868601.1:n.4424+149_4424+150insACA
XM_024447074.1:c.7652+149_7652+150insACA	XP_024302842.1:n.7652+149_7652+150insACA
NM_017890.5:c.8867+149_8867+150insACA MANE Plus Clinical	NP_060360.3:n.8867+149_8867+150insACA
NM_152564.5:c.8792+149_8792+150insACA MANE Select	NP_689777.3:n.8792+149_8792+150insACA