Canonical Allele Identifier: CA2694424073

Gene: PSMD10

Linked Data

• gnomAD v4: X-108084432-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084432C>A , CM000685.2:g.108084432C>A	GRCh38
NC_000023.10:g.107327662C>A , CM000685.1:g.107327662C>A	GRCh37
NC_000023.9:g.107214318C>A	NCBI36
NG_012521.1:g.12187G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*542G>T MANE Select	ENSP00000217958.3:n.*542G>T
ENST00000217958.7:c.*542G>T	ENSP00000217958.3:n.*542G>T
NM_002814.3:c.*542G>T	NP_002805.1:n.*542G>T
NM_170750.2:c.*688G>T	NP_736606.1:n.*688G>T
NM_002814.4:c.*542G>T MANE Select	NP_002805.1:n.*542G>T
NM_170750.3:c.*688G>T	NP_736606.1:n.*688G>T