Canonical Allele Identifier: CA397710253

Gene: VPS53

Linked Data

• MyVariant Identifiers: chr17:g.436095A>G (hg19) ; chr17:g.532855A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.532855A>G , CM000679.2:g.532855A>G	GRCh38
NC_000017.10:g.436095A>G , CM000679.1:g.436095A>G	GRCh37
NC_000017.9:g.382845A>G	NCBI36
NG_034190.1:g.187002T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291074.10:c.1985T>C	ENSP00000291074.5:p.Val662Ala
ENST00000437048.7:c.2072T>C MANE Select	ENSP00000401435.2:p.Val691Ala
ENST00000571805.6:c.2072T>C	ENSP00000459312.1:p.Val691Ala
ENST00000572334.7:c.1703T>C	ENSP00000506188.1:p.Val568Ala
ENST00000679817.1:c.302T>C	ENSP00000505032.1:p.Val101Ala
ENST00000680128.1:c.1868T>C	ENSP00000506159.1:p.Val623Ala
ENST00000680465.1:c.2072T>C	ENSP00000505997.1:p.Val691Ala
ENST00000680641.1:c.*3321T>C	ENSP00000505237.1:n.*3321T>C
ENST00000680704.1:c.1703T>C	ENSP00000506453.1:p.Val568Ala
ENST00000680872.1:c.*1198T>C	ENSP00000506605.1:n.*1198T>C
ENST00000681050.1:c.285T>C
ENST00000681096.1:c.1613T>C	ENSP00000506052.1:p.Val538Ala
ENST00000681103.1:c.302T>C	ENSP00000505892.1:p.Val101Ala
ENST00000681160.1:c.1703T>C	ENSP00000504905.1:p.Val568Ala
ENST00000681317.1:c.2015+4173T>C	ENSP00000505190.1:n.2015+4173T>C
ENST00000681478.1:c.*1892T>C	ENSP00000505041.1:n.*1892T>C
ENST00000681510.1:c.1922T>C	ENSP00000505594.1:p.Val641Ala
ENST00000681600.1:n.1167T>C
ENST00000681661.1:c.*1053T>C	ENSP00000506596.1:n.*1053T>C
ENST00000681858.1:c.302T>C	ENSP00000505044.1:p.Val101Ala
ENST00000681917.1:c.1541T>C	ENSP00000505944.1:p.Val514Ala
ENST00000681943.1:c.1790T>C	ENSP00000504889.1:n.1790T>C
ENST00000681946.1:c.*1053T>C	ENSP00000505563.1:n.*1053T>C
ENST00000291074.9:c.1985T>C	ENSP00000291074.5:p.Val662Ala
ENST00000389040.9:c.1875T>C	ENSP00000373692.5:n.1875T>C
ENST00000401468.7:c.1241T>C	ENSP00000384294.3:p.Val414Ala
ENST00000437048.6:c.2072T>C	ENSP00000401435.2:p.Val691Ala
ENST00000570771.1:n.139T>C
ENST00000571805.5:c.2072T>C	ENSP00000459312.1:p.Val691Ala
ENST00000573028.5:c.*1519T>C	ENSP00000458311.1:n.*1519T>C
ENST00000574029.5:c.207-15216T>C	ENSP00000459159.1:n.207-15216T>C
ENST00000576149.5:n.1842T>C
NM_001128159.2:c.2072T>C	NP_001121631.1:p.Val691Ala
NM_018289.3:c.1985T>C	NP_060759.2:p.Val662Ala
XM_011523953.1:c.1478T>C	XP_011522255.1:p.Val493Ala
XR_934061.1:n.2369T>C
XR_934133.1:n.291-7534A>G
NM_001366253.1:c.2072T>C	NP_001353182.1:p.Val691Ala
NM_001366254.1:c.1478T>C	NP_001353183.1:p.Val493Ala
XM_017024817.2:c.1922T>C	XP_016880306.1:p.Val641Ala
XM_017024818.1:c.1703T>C	XP_016880307.1:p.Val568Ala
XR_001752553.2:n.2209T>C
XR_934061.3:n.2359T>C
NM_001128159.3:c.2072T>C MANE Select	NP_001121631.1:p.Val691Ala
NM_001366253.2:c.2072T>C	NP_001353182.1:p.Val691Ala
NM_001366254.2:c.1478T>C	NP_001353183.1:p.Val493Ala
NM_018289.4:c.1985T>C	NP_060759.2:p.Val662Ala