Canonical Allele Identifier: CA2450520171
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084508_108084509delinsTA , CM000685.2:g.108084508_108084509delinsTA GRCh38
NC_000023.10:g.107327738_107327739delinsTA , CM000685.1:g.107327738_107327739delinsTA GRCh37
NC_000023.9:g.107214394_107214395delinsTA NCBI36
NG_012521.1:g.12110_12111delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*465_*466delinsTA MANE Select ENSP00000217958.3:n.*465_*466delinsTA
ENST00000217958.7:c.*465_*466delinsTA ENSP00000217958.3:n.*465_*466delinsTA
NM_002814.3:c.*465_*466delinsTA NP_002805.1:n.*465_*466delinsTA
NM_170750.2:c.*611_*612delinsTA NP_736606.1:n.*611_*612delinsTA
NM_002814.4:c.*465_*466delinsTA MANE Select NP_002805.1:n.*465_*466delinsTA
NM_170750.3:c.*611_*612delinsTA NP_736606.1:n.*611_*612delinsTA