Canonical Allele Identifier: CA2694424072

Gene: PSMD10

Linked Data

• gnomAD v4: X-108084415-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084415C>A , CM000685.2:g.108084415C>A	GRCh38
NC_000023.10:g.107327645C>A , CM000685.1:g.107327645C>A	GRCh37
NC_000023.9:g.107214301C>A	NCBI36
NG_012521.1:g.12204G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*559G>T MANE Select	ENSP00000217958.3:n.*559G>T
ENST00000217958.7:c.*559G>T	ENSP00000217958.3:n.*559G>T
NM_002814.3:c.*559G>T	NP_002805.1:n.*559G>T
NM_170750.2:c.*705G>T	NP_736606.1:n.*705G>T
NM_002814.4:c.*559G>T MANE Select	NP_002805.1:n.*559G>T
NM_170750.3:c.*705G>T	NP_736606.1:n.*705G>T