Canonical Allele Identifier: CA371875720

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100789092T>C (hg19) ; chr8:g.99776864T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99776864T>C , CM000670.2:g.99776864T>C	GRCh38
NC_000008.10:g.100789092T>C , CM000670.1:g.100789092T>C	GRCh37
NC_000008.9:g.100858268T>C	NCBI36
NG_007098.2:g.768599T>C , LRG_351:g.768599T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682153.1:c.7412T>C	ENSP00000507923.1:p.Phe2471Ser
ENST00000682358.1:n.7482T>C
ENST00000683334.1:c.*3094T>C	ENSP00000507369.1:n.*3094T>C
ENST00000357162.7:c.7337T>C MANE Select	ENSP00000349685.2:p.Phe2446Ser
ENST00000358544.7:c.7412T>C MANE Plus Clinical	ENSP00000351346.2:p.Phe2471Ser
ENST00000357162.6:c.7337T>C	ENSP00000349685.2:p.Phe2446Ser
ENST00000358544.6:c.7412T>C	ENSP00000351346.2:p.Phe2471Ser
ENST00000518569.1:n.378-1818T>C
NM_017890.4:c.7412T>C , LRG_351t1:c.7412T>C	NP_060360.3:p.Phe2471Ser
NM_152564.4:c.7337T>C , LRG_351t2:c.7337T>C	NP_689777.3:p.Phe2446Ser
XM_005250800.2:c.7412T>C	XP_005250857.1:p.Phe2471Ser
XM_005250801.3:c.7412T>C	XP_005250858.1:p.Phe2471Ser
XM_011516848.1:c.7409T>C	XP_011515150.1:p.Phe2470Ser
XM_011516849.1:c.7334T>C	XP_011515151.1:p.Phe2445Ser
XM_011516850.1:c.7034T>C	XP_011515152.1:p.Phe2345Ser
XM_011516851.1:c.4298T>C	XP_011515153.1:p.Phe1433Ser
XM_011516852.1:c.4298T>C	XP_011515154.1:p.Phe1433Ser
XM_011516853.1:c.7412T>C	XP_011515155.1:p.Phe2471Ser
XM_011516854.1:c.3191T>C	XP_011515156.1:p.Phe1064Ser
XR_928446.1:n.1830+5614A>G
XM_005250800.3:c.7412T>C	XP_005250857.1:p.Phe2471Ser
XM_005250801.5:c.7412T>C	XP_005250858.1:p.Phe2471Ser
XM_011516848.2:c.7409T>C	XP_011515150.1:p.Phe2470Ser
XM_011516849.2:c.7334T>C	XP_011515151.1:p.Phe2445Ser
XM_011516850.2:c.7034T>C	XP_011515152.1:p.Phe2345Ser
XM_011516851.2:c.4298T>C	XP_011515153.1:p.Phe1433Ser
XM_011516852.2:c.4298T>C	XP_011515154.1:p.Phe1433Ser
XM_011516853.2:c.7412T>C	XP_011515155.1:p.Phe2471Ser
XM_011516854.2:c.3191T>C	XP_011515156.1:p.Phe1064Ser
XM_017013109.1:c.7217T>C	XP_016868598.1:p.Phe2406Ser
XM_017013111.1:c.4298T>C	XP_016868600.1:p.Phe1433Ser
XM_017013112.1:c.2969T>C	XP_016868601.1:p.Phe990Ser
XM_024447074.1:c.6197T>C	XP_024302842.1:p.Phe2066Ser
NM_017890.5:c.7412T>C MANE Plus Clinical	NP_060360.3:p.Phe2471Ser
NM_152564.5:c.7337T>C MANE Select	NP_689777.3:p.Phe2446Ser