Canonical Allele Identifier: CA1917659946

Gene: VPS26A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69171765A= , CM000672.2:g.69171765A=	GRCh38
NC_000010.10:g.70931521A= , CM000672.1:g.70931521A=	GRCh37
NC_000010.9:g.70601527A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000263559.11:c.*496A= MANE Select	ENSP00000263559.6:n.*496A=
ENST00000263559.10:c.*496A=	ENSP00000263559.6:n.*496A=
ENST00000373382.5:c.*496A=	ENSP00000362480.1:n.*496A=
ENST00000395098.5:c.*581A=	ENSP00000378532.1:n.*581A=
NM_001035260.1:c.*581A=	NP_001030337.1:n.*581A=
NM_004896.3:c.*496A=	NP_004887.2:n.*496A=
XM_011540378.1:c.*496A=	XP_011538680.1:n.*496A=
NM_001035260.2:c.*581A=	NP_001030337.1:n.*581A=
NM_001318944.1:c.*496A=	NP_001305873.1:n.*496A=
NM_001318945.1:c.*496A=	NP_001305874.1:n.*496A=
NM_001318946.1:c.*496A=	NP_001305875.1:n.*496A=
NM_004896.4:c.*496A=	NP_004887.2:n.*496A=
NM_004896.5:c.*496A= MANE Select	NP_004887.2:n.*496A=
NM_001318944.2:c.*496A=	NP_001305873.1:n.*496A=
NM_001318945.2:c.*496A=	NP_001305874.1:n.*496A=
NM_001318946.2:c.*496A=	NP_001305875.1:n.*496A=
NM_001035260.3:c.*581A=	NP_001030337.1:n.*581A=