Canonical Allele Identifier: CA2822885154

Gene: PSMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084364_108084365insCACTTAGCCTGTGATGAGGAGAGAGT , CM000685.2:g.108084364_108084365insCACTTAGCCTGTGATGAGGAGAGAGT	GRCh38
NC_000023.10:g.107327594_107327595insCACTTAGCCTGTGATGAGGAGAGAGT , CM000685.1:g.107327594_107327595insCACTTAGCCTGTGATGAGGAGAGAGT	GRCh37
NC_000023.9:g.107214250_107214251insCACTTAGCCTGTGATGAGGAGAGAGT	NCBI36
NG_012521.1:g.12254_12255insACTCTCTCCTCATCACAGGCTAAGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*609_*610insACTCTCTCCTCATCACAGGCTAAGTG MANE Select	ENSP00000217958.3:n.*609_*610insACTCTCTCCTCATCACAGGCTAAGTG
ENST00000217958.7:c.*609_*610insACTCTCTCCTCATCACAGGCTAAGTG	ENSP00000217958.3:n.*609_*610insACTCTCTCCTCATCACAGGCTAAGTG
NM_002814.3:c.*609_*610insACTCTCTCCTCATCACAGGCTAAGTG	NP_002805.1:n.*609_*610insACTCTCTCCTCATCACAGGCTAAGTG
NM_170750.2:c.*755_*756insACTCTCTCCTCATCACAGGCTAAGTG	NP_736606.1:n.*755_*756insACTCTCTCCTCATCACAGGCTAAGTG
NM_002814.4:c.*609_*610insACTCTCTCCTCATCACAGGCTAAGTG MANE Select	NP_002805.1:n.*609_*610insACTCTCTCCTCATCACAGGCTAAGTG
NM_170750.3:c.*755_*756insACTCTCTCCTCATCACAGGCTAAGTG	NP_736606.1:n.*755_*756insACTCTCTCCTCATCACAGGCTAAGTG