Canonical Allele Identifier: CA413841520

Gene: PSMD10

Linked Data

• gnomAD v4: X-108084992-C-A
• MyVariant Identifiers: chrX:g.107328222C>A (hg19) ; chrX:g.108084992C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084992C>A , CM000685.2:g.108084992C>A	GRCh38
NC_000023.10:g.107328222C>A , CM000685.1:g.107328222C>A	GRCh37
NC_000023.9:g.107214878C>A	NCBI36
NG_012521.1:g.11627G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.663G>T MANE Select	ENSP00000217958.3:p.Lys221Asn
ENST00000217958.7:c.663G>T	ENSP00000217958.3:p.Lys221Asn
ENST00000340200.5:c.564G>T	ENSP00000345963.5:p.Lys188Asn
ENST00000361815.9:c.*128G>T	ENSP00000354906.5:n.*128G>T
ENST00000372295.5:c.540G>T	ENSP00000361369.1:p.Lys180Asn
ENST00000372296.5:c.*128G>T	ENSP00000361370.1:n.*128G>T
NM_002814.3:c.663G>T	NP_002805.1:p.Lys221Asn
NM_170750.2:c.*128G>T	NP_736606.1:n.*128G>T
NM_002814.4:c.663G>T MANE Select	NP_002805.1:p.Lys221Asn
NM_170750.3:c.*128G>T	NP_736606.1:n.*128G>T