Canonical Allele Identifier: CA397710347

Gene: VPS53

Linked Data

• MyVariant Identifiers: chr17:g.436119A>G (hg19) ; chr17:g.532879A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.532879A>G , CM000679.2:g.532879A>G	GRCh38
NC_000017.10:g.436119A>G , CM000679.1:g.436119A>G	GRCh37
NC_000017.9:g.382869A>G	NCBI36
NG_034190.1:g.186978T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291074.10:c.1961T>C	ENSP00000291074.5:p.Phe654Ser
ENST00000437048.7:c.2048T>C MANE Select	ENSP00000401435.2:p.Phe683Ser
ENST00000571805.6:c.2048T>C	ENSP00000459312.1:p.Phe683Ser
ENST00000572334.7:c.1679T>C	ENSP00000506188.1:p.Phe560Ser
ENST00000679817.1:c.278T>C	ENSP00000505032.1:p.Phe93Ser
ENST00000680128.1:c.1844T>C	ENSP00000506159.1:p.Phe615Ser
ENST00000680465.1:c.2048T>C	ENSP00000505997.1:p.Phe683Ser
ENST00000680641.1:c.*3297T>C	ENSP00000505237.1:n.*3297T>C
ENST00000680704.1:c.1679T>C	ENSP00000506453.1:p.Phe560Ser
ENST00000680872.1:c.*1174T>C	ENSP00000506605.1:n.*1174T>C
ENST00000681050.1:c.261T>C
ENST00000681096.1:c.1589T>C	ENSP00000506052.1:p.Phe530Ser
ENST00000681103.1:c.278T>C	ENSP00000505892.1:p.Phe93Ser
ENST00000681160.1:c.1679T>C	ENSP00000504905.1:p.Phe560Ser
ENST00000681317.1:c.2015+4149T>C	ENSP00000505190.1:n.2015+4149T>C
ENST00000681478.1:c.*1868T>C	ENSP00000505041.1:n.*1868T>C
ENST00000681510.1:c.1898T>C	ENSP00000505594.1:p.Phe633Ser
ENST00000681600.1:n.1143T>C
ENST00000681661.1:c.*1029T>C	ENSP00000506596.1:n.*1029T>C
ENST00000681858.1:c.278T>C	ENSP00000505044.1:p.Phe93Ser
ENST00000681917.1:c.1517T>C	ENSP00000505944.1:p.Phe506Ser
ENST00000681943.1:c.1766T>C	ENSP00000504889.1:n.1766T>C
ENST00000681946.1:c.*1029T>C	ENSP00000505563.1:n.*1029T>C
ENST00000291074.9:c.1961T>C	ENSP00000291074.5:p.Phe654Ser
ENST00000389040.9:c.1851T>C	ENSP00000373692.5:n.1851T>C
ENST00000401468.7:c.1217T>C	ENSP00000384294.3:p.Phe406Ser
ENST00000437048.6:c.2048T>C	ENSP00000401435.2:p.Phe683Ser
ENST00000570771.1:n.115T>C
ENST00000571805.5:c.2048T>C	ENSP00000459312.1:p.Phe683Ser
ENST00000573028.5:c.*1495T>C	ENSP00000458311.1:n.*1495T>C
ENST00000574029.5:c.207-15240T>C	ENSP00000459159.1:n.207-15240T>C
ENST00000576149.5:n.1818T>C
NM_001128159.2:c.2048T>C	NP_001121631.1:p.Phe683Ser
NM_018289.3:c.1961T>C	NP_060759.2:p.Phe654Ser
XM_011523953.1:c.1454T>C	XP_011522255.1:p.Phe485Ser
XR_934061.1:n.2345T>C
XR_934133.1:n.291-7510A>G
NM_001366253.1:c.2048T>C	NP_001353182.1:p.Phe683Ser
NM_001366254.1:c.1454T>C	NP_001353183.1:p.Phe485Ser
XM_017024817.2:c.1898T>C	XP_016880306.1:p.Phe633Ser
XM_017024818.1:c.1679T>C	XP_016880307.1:p.Phe560Ser
XR_001752553.2:n.2185T>C
XR_934061.3:n.2335T>C
NM_001128159.3:c.2048T>C MANE Select	NP_001121631.1:p.Phe683Ser
NM_001366253.2:c.2048T>C	NP_001353182.1:p.Phe683Ser
NM_001366254.2:c.1454T>C	NP_001353183.1:p.Phe485Ser
NM_018289.4:c.1961T>C	NP_060759.2:p.Phe654Ser