Canonical Allele Identifier: CA2450520325
Gene: PSMD10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085018_108085019delinsTG , CM000685.2:g.108085018_108085019delinsTG GRCh38
NC_000023.10:g.107328248_107328249delinsTG , CM000685.1:g.107328248_107328249delinsTG GRCh37
NC_000023.9:g.107214904_107214905delinsTG NCBI36
NG_012521.1:g.11600_11601delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.636_637delinsCA MANE Select ENSP00000217958.3:p.Ala212=
ENST00000217958.7:c.636_637delinsCA ENSP00000217958.3:p.Ala212=
ENST00000340200.5:c.537_538delinsCA ENSP00000345963.5:p.Ala179=
ENST00000361815.9:c.*101_*102delinsCA ENSP00000354906.5:n.*101_*102delinsCA
ENST00000372295.5:c.513_514delinsCA ENSP00000361369.1:p.Ala171=
ENST00000372296.5:c.*101_*102delinsCA ENSP00000361370.1:n.*101_*102delinsCA
NM_002814.3:c.636_637delinsCA NP_002805.1:p.Ala212=
NM_170750.2:c.*101_*102delinsCA NP_736606.1:n.*101_*102delinsCA
NM_002814.4:c.636_637delinsCA MANE Select NP_002805.1:p.Ala212=
NM_170750.3:c.*101_*102delinsCA NP_736606.1:n.*101_*102delinsCA
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