Canonical Allele Identifier: CA413841617

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328268T>A (hg19) ; chrX:g.108085038T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085038T>A , CM000685.2:g.108085038T>A	GRCh38
NC_000023.10:g.107328268T>A , CM000685.1:g.107328268T>A	GRCh37
NC_000023.9:g.107214924T>A	NCBI36
NG_012521.1:g.11581A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.617A>T MANE Select	ENSP00000217958.3:p.Lys206Met
ENST00000217958.7:c.617A>T	ENSP00000217958.3:p.Lys206Met
ENST00000340200.5:c.518A>T	ENSP00000345963.5:p.Lys173Met
ENST00000361815.9:c.*82A>T	ENSP00000354906.5:n.*82A>T
ENST00000372295.5:c.494A>T	ENSP00000361369.1:p.Lys165Met
ENST00000372296.5:c.*82A>T	ENSP00000361370.1:n.*82A>T
NM_002814.3:c.617A>T	NP_002805.1:p.Lys206Met
NM_170750.2:c.*82A>T	NP_736606.1:n.*82A>T
NM_002814.4:c.617A>T MANE Select	NP_002805.1:p.Lys206Met
NM_170750.3:c.*82A>T	NP_736606.1:n.*82A>T