Canonical Allele Identifier: CA2694424239

Gene: PSMD10

Linked Data

• gnomAD v4: X-108084847-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084847G>T , CM000685.2:g.108084847G>T	GRCh38
NC_000023.10:g.107328077G>T , CM000685.1:g.107328077G>T	GRCh37
NC_000023.9:g.107214733G>T	NCBI36
NG_012521.1:g.11772C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*127C>A MANE Select	ENSP00000217958.3:n.*127C>A
ENST00000217958.7:c.*127C>A	ENSP00000217958.3:n.*127C>A
ENST00000340200.5:c.709C>A	ENSP00000345963.5:n.709C>A
ENST00000361815.9:c.*273C>A	ENSP00000354906.5:n.*273C>A
ENST00000372295.5:c.*127C>A	ENSP00000361369.1:n.*127C>A
ENST00000372296.5:c.*273C>A	ENSP00000361370.1:n.*273C>A
NM_002814.3:c.*127C>A	NP_002805.1:n.*127C>A
NM_170750.2:c.*273C>A	NP_736606.1:n.*273C>A
NM_002814.4:c.*127C>A MANE Select	NP_002805.1:n.*127C>A
NM_170750.3:c.*273C>A	NP_736606.1:n.*273C>A