Canonical Allele Identifier: CA413841808

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328351T>A (hg19) ; chrX:g.108085121T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085121T>A , CM000685.2:g.108085121T>A	GRCh38
NC_000023.10:g.107328351T>A , CM000685.1:g.107328351T>A	GRCh37
NC_000023.9:g.107215007T>A	NCBI36
NG_012521.1:g.11498A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.534A>T MANE Select	ENSP00000217958.3:p.Leu178Phe
ENST00000217958.7:c.534A>T	ENSP00000217958.3:p.Leu178Phe
ENST00000340200.5:c.435A>T	ENSP00000345963.5:p.Leu145Phe
ENST00000361815.9:c.455A>T	ENSP00000354906.5:p.Ter152Leu
ENST00000372295.5:c.411A>T	ENSP00000361369.1:p.Leu137Phe
ENST00000372296.5:c.332A>T	ENSP00000361370.1:p.Ter111Leu
NM_002814.3:c.534A>T	NP_002805.1:p.Leu178Phe
NM_170750.2:c.455A>T	NP_736606.1:p.Ter152Leu
NM_002814.4:c.534A>T MANE Select	NP_002805.1:p.Leu178Phe
NM_170750.3:c.455A>T	NP_736606.1:p.Ter152Leu