Canonical Allele Identifier: CA371790555

Gene: VPS13B

Linked Data

• ClinVar Variation Id: 844524
• ClinVar RCV Id: RCV001047393
• dbSNP Id: rs1451352816
• gnomAD v2: 8-100874090-C-T
• gnomAD v3: 8-99861862-C-T
• gnomAD v4: 8-99861862-C-T
• MyVariant Identifiers: chr8:g.100874090C>T (hg19) ; chr8:g.100874090_100874093delinsTAGG (hg19) ; chr8:g.99861862C>T (hg38) ; chr8:g.99861862_99861865delinsTAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99861862C>T , CM000670.2:g.99861862C>T	GRCh38
NC_000008.10:g.100874090C>T , CM000670.1:g.100874090C>T	GRCh37
NC_000008.9:g.100943266C>T	NCBI36
NG_007098.2:g.853597C>T , LRG_351:g.853597C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*300C>T	ENSP00000507923.1:n.*300C>T
ENST00000682358.1:n.11276C>T
ENST00000683334.1:c.*6888C>T	ENSP00000507369.1:n.*6888C>T
ENST00000357162.7:c.11131C>T MANE Select	ENSP00000349685.2:p.Gln3711Ter
ENST00000358544.7:c.11206C>T MANE Plus Clinical	ENSP00000351346.2:p.Gln3736Ter
ENST00000357162.6:c.11131C>T	ENSP00000349685.2:p.Gln3711Ter
ENST00000358544.6:c.11206C>T	ENSP00000351346.2:p.Gln3736Ter
NM_017890.4:c.11206C>T , LRG_351t1:c.11206C>T	NP_060360.3:p.Gln3736Ter
NM_152564.4:c.11131C>T , LRG_351t2:c.11131C>T	NP_689777.3:p.Gln3711Ter
XM_005250800.2:c.11206C>T	XP_005250857.1:p.Gln3736Ter
XM_005250801.3:c.11206C>T	XP_005250858.1:p.Gln3736Ter
XM_011516848.1:c.11203C>T	XP_011515150.1:p.Gln3735Ter
XM_011516849.1:c.11128C>T	XP_011515151.1:p.Gln3710Ter
XM_011516850.1:c.10828C>T	XP_011515152.1:p.Gln3610Ter
XM_011516851.1:c.8092C>T	XP_011515153.1:p.Gln2698Ter
XM_011516852.1:c.8092C>T	XP_011515154.1:p.Gln2698Ter
XM_011516854.1:c.6985C>T	XP_011515156.1:p.Gln2329Ter
XM_005250800.3:c.11206C>T	XP_005250857.1:p.Gln3736Ter
XM_005250801.5:c.11206C>T	XP_005250858.1:p.Gln3736Ter
XM_011516848.2:c.11203C>T	XP_011515150.1:p.Gln3735Ter
XM_011516849.2:c.11128C>T	XP_011515151.1:p.Gln3710Ter
XM_011516850.2:c.10828C>T	XP_011515152.1:p.Gln3610Ter
XM_011516851.2:c.8092C>T	XP_011515153.1:p.Gln2698Ter
XM_011516852.2:c.8092C>T	XP_011515154.1:p.Gln2698Ter
XM_011516854.2:c.6985C>T	XP_011515156.1:p.Gln2329Ter
XM_017013109.1:c.11011C>T	XP_016868598.1:p.Gln3671Ter
XM_017013111.1:c.8092C>T	XP_016868600.1:p.Gln2698Ter
XM_017013112.1:c.6763C>T	XP_016868601.1:p.Gln2255Ter
XM_024447074.1:c.9991C>T	XP_024302842.1:p.Gln3331Ter
NM_017890.5:c.11206C>T MANE Plus Clinical	NP_060360.3:p.Gln3736Ter
NM_152564.5:c.11131C>T MANE Select	NP_689777.3:p.Gln3711Ter