Canonical Allele Identifier: CA2694424292

Gene: PSMD10

Linked Data

• gnomAD v4: X-108084961-AAATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084962_108084965del , CM000685.2:g.108084962_108084965del	GRCh38
NC_000023.10:g.107328192_107328195del , CM000685.1:g.107328192_107328195del	GRCh37
NC_000023.9:g.107214848_107214851del	NCBI36
NG_012521.1:g.11654_11657del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*9_*12del MANE Select	ENSP00000217958.3:n.*9_*12del
ENST00000217958.7:c.*9_*12del	ENSP00000217958.3:n.*9_*12del
ENST00000340200.5:c.591_594del	ENSP00000345963.5:n.591_594del
ENST00000361815.9:c.*155_*158del	ENSP00000354906.5:n.*155_*158del
ENST00000372295.5:c.*9_*12del	ENSP00000361369.1:n.*9_*12del
ENST00000372296.5:c.*155_*158del	ENSP00000361370.1:n.*155_*158del
NM_002814.3:c.*9_*12del	NP_002805.1:n.*9_*12del
NM_170750.2:c.*155_*158del	NP_736606.1:n.*155_*158del
NM_002814.4:c.*9_*12del MANE Select	NP_002805.1:n.*9_*12del
NM_170750.3:c.*155_*158del	NP_736606.1:n.*155_*158del