Canonical Allele Identifier: CA2694424294

Gene: PSMD10

Linked Data

• gnomAD v4: X-108084969-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084969G>A , CM000685.2:g.108084969G>A	GRCh38
NC_000023.10:g.107328199G>A , CM000685.1:g.107328199G>A	GRCh37
NC_000023.9:g.107214855G>A	NCBI36
NG_012521.1:g.11650C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*5C>T MANE Select	ENSP00000217958.3:n.*5C>T
ENST00000217958.7:c.*5C>T	ENSP00000217958.3:n.*5C>T
ENST00000340200.5:c.587C>T	ENSP00000345963.5:n.587C>T
ENST00000361815.9:c.*151C>T	ENSP00000354906.5:n.*151C>T
ENST00000372295.5:c.*5C>T	ENSP00000361369.1:n.*5C>T
ENST00000372296.5:c.*151C>T	ENSP00000361370.1:n.*151C>T
NM_002814.3:c.*5C>T	NP_002805.1:n.*5C>T
NM_170750.2:c.*151C>T	NP_736606.1:n.*151C>T
NM_002814.4:c.*5C>T MANE Select	NP_002805.1:n.*5C>T
NM_170750.3:c.*151C>T	NP_736606.1:n.*151C>T