Canonical Allele Identifier: CA286395377

Gene: VPS53

Linked Data

• dbSNP Id: rs960945488
• gnomAD v4: 17-532768-C-G
• MyVariant Identifiers: chr17:g.436008C>G (hg19) ; chr17:g.532768C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.532768C>G , CM000679.2:g.532768C>G	GRCh38
NC_000017.10:g.436008C>G , CM000679.1:g.436008C>G	GRCh37
NC_000017.9:g.382758C>G	NCBI36
NG_034190.1:g.187089G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291074.10:c.*59G>C	ENSP00000291074.5:n.*59G>C
ENST00000437048.7:c.2085+74G>C MANE Select	ENSP00000401435.2:n.2085+74G>C
ENST00000571805.6:c.*59G>C	ENSP00000459312.1:n.*59G>C
ENST00000679817.1:c.*59G>C	ENSP00000505032.1:n.*59G>C
ENST00000680128.1:c.*59G>C	ENSP00000506159.1:n.*59G>C
ENST00000680465.1:c.2085+74G>C	ENSP00000505997.1:n.2085+74G>C
ENST00000680641.1:c.*3334+74G>C	ENSP00000505237.1:n.*3334+74G>C
ENST00000680872.1:c.*1211+74G>C	ENSP00000506605.1:n.*1211+74G>C
ENST00000681050.1:c.298+74G>C
ENST00000681096.1:c.*59G>C	ENSP00000506052.1:n.*59G>C
ENST00000681103.1:c.315+74G>C	ENSP00000505892.1:n.315+74G>C
ENST00000681160.1:c.1716+74G>C	ENSP00000504905.1:n.1716+74G>C
ENST00000681317.1:c.2015+4260G>C	ENSP00000505190.1:n.2015+4260G>C
ENST00000681478.1:c.*1979G>C	ENSP00000505041.1:n.*1979G>C
ENST00000681510.1:c.1935+74G>C	ENSP00000505594.1:n.1935+74G>C
ENST00000681600.1:n.1180+74G>C
ENST00000681661.1:c.*1066+74G>C	ENSP00000506596.1:n.*1066+74G>C
ENST00000681858.1:c.315+74G>C	ENSP00000505044.1:n.315+74G>C
ENST00000681917.1:c.1554+74G>C	ENSP00000505944.1:n.1554+74G>C
ENST00000681943.1:c.1803+74G>C	ENSP00000504889.1:n.1803+74G>C
ENST00000681946.1:c.*1066+74G>C	ENSP00000505563.1:n.*1066+74G>C
ENST00000291074.9:c.*59G>C	ENSP00000291074.5:n.*59G>C
ENST00000437048.6:c.2085+74G>C	ENSP00000401435.2:n.2085+74G>C
ENST00000570771.1:n.152+74G>C
ENST00000571805.5:c.*59G>C	ENSP00000459312.1:n.*59G>C
ENST00000573028.5:c.*1606G>C	ENSP00000458311.1:n.*1606G>C
ENST00000574029.5:c.207-15129G>C	ENSP00000459159.1:n.207-15129G>C
ENST00000576149.5:n.1855+74G>C
NM_001128159.2:c.2085+74G>C	NP_001121631.1:n.2085+74G>C
NM_018289.3:c.*59G>C	NP_060759.2:n.*59G>C
XM_011523953.1:c.*59G>C	XP_011522255.1:n.*59G>C
XR_934061.1:n.2382+74G>C
XR_934133.1:n.291-7621C>G
NM_001366253.1:c.*59G>C	NP_001353182.1:n.*59G>C
NM_001366254.1:c.*59G>C	NP_001353183.1:n.*59G>C
XM_017024817.2:c.1935+74G>C	XP_016880306.1:n.1935+74G>C
XM_017024818.1:c.1716+74G>C	XP_016880307.1:n.1716+74G>C
XR_001752553.2:n.2222+74G>C
XR_934061.3:n.2372+74G>C
NM_001128159.3:c.2085+74G>C MANE Select	NP_001121631.1:n.2085+74G>C
NM_001366253.2:c.*59G>C	NP_001353182.1:n.*59G>C
NM_001366254.2:c.*59G>C	NP_001353183.1:n.*59G>C
NM_018289.4:c.*59G>C	NP_060759.2:n.*59G>C