Canonical Allele Identifier: CA1917659967

Gene: VPS26A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69171813C= , CM000672.2:g.69171813C=	GRCh38
NC_000010.10:g.70931569C= , CM000672.1:g.70931569C=	GRCh37
NC_000010.9:g.70601575C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263559.11:c.*544C= MANE Select	ENSP00000263559.6:n.*544C=
ENST00000263559.10:c.*544C=	ENSP00000263559.6:n.*544C=
ENST00000373382.5:c.*544C=	ENSP00000362480.1:n.*544C=
ENST00000395098.5:c.*629C=	ENSP00000378532.1:n.*629C=
NM_001035260.1:c.*629C=	NP_001030337.1:n.*629C=
NM_004896.3:c.*544C=	NP_004887.2:n.*544C=
XM_011540378.1:c.*544C=	XP_011538680.1:n.*544C=
NM_001035260.2:c.*629C=	NP_001030337.1:n.*629C=
NM_001318944.1:c.*544C=	NP_001305873.1:n.*544C=
NM_001318945.1:c.*544C=	NP_001305874.1:n.*544C=
NM_001318946.1:c.*544C=	NP_001305875.1:n.*544C=
NM_004896.4:c.*544C=	NP_004887.2:n.*544C=
NM_004896.5:c.*544C= MANE Select	NP_004887.2:n.*544C=
NM_001318944.2:c.*544C=	NP_001305873.1:n.*544C=
NM_001318945.2:c.*544C=	NP_001305874.1:n.*544C=
NM_001318946.2:c.*544C=	NP_001305875.1:n.*544C=
NM_001035260.3:c.*629C=	NP_001030337.1:n.*629C=