Canonical Allele Identifier: CA913128160
Gene: VPS13B HGNC NCBI
COX6C HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.100887795dup (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.99875567dup , CM000670.2:g.99875567dup GRCh38
NC_000008.10:g.100887795dup , CM000670.1:g.100887795dup GRCh37
NC_000008.9:g.100956971dup NCBI36
NG_007098.2:g.867302dup , LRG_351:g.867302dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682153.1:c.*1624dup (VPS13B) ENSP00000507923.1:n.*1624dup
ENST00000682358.1:n.12600dup (VPS13B)
ENST00000683334.1:c.*7652dup (VPS13B) ENSP00000507369.1:n.*7652dup
ENST00000357162.7:c.11895dup (VPS13B) MANE Select ENSP00000349685.2:p.Lys3966Ter
ENST00000358544.7:c.11970dup (VPS13B) MANE Plus Clinical ENSP00000351346.2:p.Lys3991Ter
ENST00000357162.6:c.11895dup (VPS13B) ENSP00000349685.2:p.Lys3966Ter
ENST00000358544.6:c.11970dup (VPS13B) ENSP00000351346.2:p.Lys3991Ter
ENST00000493587.1:n.1472dup (VPS13B)
ENST00000520517.5:c.*142-474dup (COX6C) ENSP00000429991.1:n.*142-474dup
ENST00000522934.5:c.*142-2273dup (COX6C) ENSP00000428702.1:n.*142-2273dup
NM_017890.4:c.11970dup , LRG_351t1:c.11970dup (VPS13B) NP_060360.3:p.Lys3991Ter
NM_152564.4:c.11895dup , LRG_351t2:c.11895dup (VPS13B) NP_689777.3:p.Lys3966Ter
XM_005250800.2:c.11970dup (VPS13B) XP_005250857.1:p.Lys3991Ter
XM_005250801.3:c.11970dup (VPS13B) XP_005250858.1:p.Lys3991Ter
XM_011516848.1:c.11967dup (VPS13B) XP_011515150.1:p.Lys3990Ter
XM_011516849.1:c.11892dup (VPS13B) XP_011515151.1:p.Lys3965Ter
XM_011516850.1:c.11592dup (VPS13B) XP_011515152.1:p.Lys3865Ter
XM_011516851.1:c.8856dup (VPS13B) XP_011515153.1:p.Lys2953Ter
XM_011516852.1:c.8856dup (VPS13B) XP_011515154.1:p.Lys2953Ter
XM_011516854.1:c.7749dup (VPS13B) XP_011515156.1:p.Lys2584Ter
XM_005250800.3:c.11970dup (VPS13B) XP_005250857.1:p.Lys3991Ter
XM_005250801.5:c.11970dup (VPS13B) XP_005250858.1:p.Lys3991Ter
XM_011516848.2:c.11967dup (VPS13B) XP_011515150.1:p.Lys3990Ter
XM_011516849.2:c.11892dup (VPS13B) XP_011515151.1:p.Lys3965Ter
XM_011516850.2:c.11592dup (VPS13B) XP_011515152.1:p.Lys3865Ter
XM_011516851.2:c.8856dup (VPS13B) XP_011515153.1:p.Lys2953Ter
XM_011516852.2:c.8856dup (VPS13B) XP_011515154.1:p.Lys2953Ter
XM_011516854.2:c.7749dup (VPS13B) XP_011515156.1:p.Lys2584Ter
XM_017013109.1:c.11775dup (VPS13B) XP_016868598.1:p.Lys3926Ter
XM_017013111.1:c.8856dup (VPS13B) XP_016868600.1:p.Lys2953Ter
XM_017013112.1:c.7527dup (VPS13B) XP_016868601.1:p.Lys2510Ter
XM_024447074.1:c.10755dup (VPS13B) XP_024302842.1:p.Lys3586Ter
NM_017890.5:c.11970dup (VPS13B) MANE Plus Clinical NP_060360.3:p.Lys3991Ter
NM_152564.5:c.11895dup (VPS13B) MANE Select NP_689777.3:p.Lys3966Ter