Canonical Allele Identifier: CA2450520189

Gene: PSMD10

Linked Data

• dbSNP Id: rs2031472970

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084557_108084561del , CM000685.2:g.108084557_108084561del	GRCh38
NC_000023.10:g.107327787_107327791del , CM000685.1:g.107327787_107327791del	GRCh37
NC_000023.9:g.107214443_107214447del	NCBI36
NG_012521.1:g.12059_12063del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*414_*418del MANE Select	ENSP00000217958.3:n.*414_*418del
ENST00000217958.7:c.*414_*418del	ENSP00000217958.3:n.*414_*418del
NM_002814.3:c.*414_*418del	NP_002805.1:n.*414_*418del
NM_170750.2:c.*560_*564del	NP_736606.1:n.*560_*564del
NM_002814.4:c.*414_*418del MANE Select	NP_002805.1:n.*414_*418del
NM_170750.3:c.*560_*564del	NP_736606.1:n.*560_*564del