Canonical Allele Identifier: CA371875569

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100789019G>T (hg19) ; chr8:g.99776791G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99776791G>T , CM000670.2:g.99776791G>T	GRCh38
NC_000008.10:g.100789019G>T , CM000670.1:g.100789019G>T	GRCh37
NC_000008.9:g.100858195G>T	NCBI36
NG_007098.2:g.768526G>T , LRG_351:g.768526G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.7339G>T	ENSP00000507923.1:p.Gly2447Cys
ENST00000682358.1:n.7409G>T
ENST00000683334.1:c.*3021G>T	ENSP00000507369.1:n.*3021G>T
ENST00000357162.7:c.7264G>T MANE Select	ENSP00000349685.2:p.Gly2422Cys
ENST00000358544.7:c.7339G>T MANE Plus Clinical	ENSP00000351346.2:p.Gly2447Cys
ENST00000357162.6:c.7264G>T	ENSP00000349685.2:p.Gly2422Cys
ENST00000358544.6:c.7339G>T	ENSP00000351346.2:p.Gly2447Cys
ENST00000518569.1:n.378-1891G>T
NM_017890.4:c.7339G>T , LRG_351t1:c.7339G>T	NP_060360.3:p.Gly2447Cys
NM_152564.4:c.7264G>T , LRG_351t2:c.7264G>T	NP_689777.3:p.Gly2422Cys
XM_005250800.2:c.7339G>T	XP_005250857.1:p.Gly2447Cys
XM_005250801.3:c.7339G>T	XP_005250858.1:p.Gly2447Cys
XM_011516848.1:c.7336G>T	XP_011515150.1:p.Gly2446Cys
XM_011516849.1:c.7261G>T	XP_011515151.1:p.Gly2421Cys
XM_011516850.1:c.6961G>T	XP_011515152.1:p.Gly2321Cys
XM_011516851.1:c.4225G>T	XP_011515153.1:p.Gly1409Cys
XM_011516852.1:c.4225G>T	XP_011515154.1:p.Gly1409Cys
XM_011516853.1:c.7339G>T	XP_011515155.1:p.Gly2447Cys
XM_011516854.1:c.3118G>T	XP_011515156.1:p.Gly1040Cys
XR_928446.1:n.1830+5687C>A
XM_005250800.3:c.7339G>T	XP_005250857.1:p.Gly2447Cys
XM_005250801.5:c.7339G>T	XP_005250858.1:p.Gly2447Cys
XM_011516848.2:c.7336G>T	XP_011515150.1:p.Gly2446Cys
XM_011516849.2:c.7261G>T	XP_011515151.1:p.Gly2421Cys
XM_011516850.2:c.6961G>T	XP_011515152.1:p.Gly2321Cys
XM_011516851.2:c.4225G>T	XP_011515153.1:p.Gly1409Cys
XM_011516852.2:c.4225G>T	XP_011515154.1:p.Gly1409Cys
XM_011516853.2:c.7339G>T	XP_011515155.1:p.Gly2447Cys
XM_011516854.2:c.3118G>T	XP_011515156.1:p.Gly1040Cys
XM_017013109.1:c.7144G>T	XP_016868598.1:p.Gly2382Cys
XM_017013111.1:c.4225G>T	XP_016868600.1:p.Gly1409Cys
XM_017013112.1:c.2896G>T	XP_016868601.1:p.Gly966Cys
XM_024447074.1:c.6124G>T	XP_024302842.1:p.Gly2042Cys
NM_017890.5:c.7339G>T MANE Plus Clinical	NP_060360.3:p.Gly2447Cys
NM_152564.5:c.7264G>T MANE Select	NP_689777.3:p.Gly2422Cys