Canonical Allele Identifier: CA517921198
Gene: PSMD10 HGNC NCBI

Linked Data

gnomAD v4: X-108085055-A-G
MyVariant Identifiers: chrX:g.107328285A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085055A>G , CM000685.2:g.108085055A>G GRCh38
NC_000023.10:g.107328285A>G , CM000685.1:g.107328285A>G GRCh37
NC_000023.9:g.107214941A>G NCBI36
NG_012521.1:g.11564T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.600T>C MANE Select ENSP00000217958.3:p.Ile200=
ENST00000217958.7:c.600T>C ENSP00000217958.3:p.Ile200=
ENST00000340200.5:c.501T>C ENSP00000345963.5:p.Ile167=
ENST00000361815.9:c.*65T>C ENSP00000354906.5:n.*65T>C
ENST00000372295.5:c.477T>C ENSP00000361369.1:p.Ile159=
ENST00000372296.5:c.*65T>C ENSP00000361370.1:n.*65T>C
NM_002814.3:c.600T>C NP_002805.1:p.Ile200=
NM_170750.2:c.*65T>C NP_736606.1:n.*65T>C
NM_002814.4:c.600T>C MANE Select NP_002805.1:p.Ile200=
NM_170750.3:c.*65T>C NP_736606.1:n.*65T>C
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