Canonical Allele Identifier: CA658420103

Gene: PSMD10

Linked Data

• COSMIC: COSN16045457

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084504_108084505insC , CM000685.2:g.108084504_108084505insC	GRCh38
NC_000023.10:g.107327734_107327735insC , CM000685.1:g.107327734_107327735insC	GRCh37
NC_000023.9:g.107214390_107214391insC	NCBI36
NG_012521.1:g.12114_12115insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*469_*470insG MANE Select	ENSP00000217958.3:n.*469_*470insG
ENST00000217958.7:c.*469_*470insG	ENSP00000217958.3:n.*469_*470insG
NM_002814.3:c.*469_*470insG	NP_002805.1:n.*469_*470insG
NM_170750.2:c.*615_*616insG	NP_736606.1:n.*615_*616insG
NM_002814.4:c.*469_*470insG MANE Select	NP_002805.1:n.*469_*470insG
NM_170750.3:c.*615_*616insG	NP_736606.1:n.*615_*616insG