Canonical Allele Identifier: CA2609431336

Gene: VPS26A

Linked Data

• gnomAD v4: 10-69171762-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69171762T>C , CM000672.2:g.69171762T>C	GRCh38
NC_000010.10:g.70931518T>C , CM000672.1:g.70931518T>C	GRCh37
NC_000010.9:g.70601524T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000263559.11:c.*493T>C MANE Select	ENSP00000263559.6:n.*493T>C
ENST00000263559.10:c.*493T>C	ENSP00000263559.6:n.*493T>C
ENST00000373382.5:c.*493T>C	ENSP00000362480.1:n.*493T>C
ENST00000395098.5:c.*578T>C	ENSP00000378532.1:n.*578T>C
NM_001035260.1:c.*578T>C	NP_001030337.1:n.*578T>C
NM_004896.3:c.*493T>C	NP_004887.2:n.*493T>C
XM_011540378.1:c.*493T>C	XP_011538680.1:n.*493T>C
NM_001035260.2:c.*578T>C	NP_001030337.1:n.*578T>C
NM_001318944.1:c.*493T>C	NP_001305873.1:n.*493T>C
NM_001318945.1:c.*493T>C	NP_001305874.1:n.*493T>C
NM_001318946.1:c.*493T>C	NP_001305875.1:n.*493T>C
NM_004896.4:c.*493T>C	NP_004887.2:n.*493T>C
NM_004896.5:c.*493T>C MANE Select	NP_004887.2:n.*493T>C
NM_001318944.2:c.*493T>C	NP_001305873.1:n.*493T>C
NM_001318945.2:c.*493T>C	NP_001305874.1:n.*493T>C
NM_001318946.2:c.*493T>C	NP_001305875.1:n.*493T>C
NM_001035260.3:c.*578T>C	NP_001030337.1:n.*578T>C