Canonical Allele Identifier: CA2738934024
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs2147940876

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085128_108085129insCCTCAGTGTCTTGGATGTTTG , CM000685.2:g.108085128_108085129insCCTCAGTGTCTTGGATGTTTG GRCh38
NC_000023.10:g.107328358_107328359insCCTCAGTGTCTTGGATGTTTG , CM000685.1:g.107328358_107328359insCCTCAGTGTCTTGGATGTTTG GRCh37
NC_000023.9:g.107215014_107215015insCCTCAGTGTCTTGGATGTTTG NCBI36
NG_012521.1:g.11490_11491insCAAACATCCAAGACACTGAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.528-2_528-1insCAAACATCCAAGACACTGAGG MANE Select ENSP00000217958.3:n.528-2_528-1insCAAACATCCAAGACACTGAGG
ENST00000217958.7:c.528-2_528-1insCAAACATCCAAGACACTGAGG ENSP00000217958.3:n.528-2_528-1insCAAACATCCAAGACACTGAGG
ENST00000340200.5:c.429-2_429-1insCAAACATCCAAGACACTGAGG ENSP00000345963.5:n.429-2_429-1insCAAACATCCAAGACACTGAGG
ENST00000361815.9:c.449-2_449-1insCAAACATCCAAGACACTGAGG ENSP00000354906.5:n.449-2_449-1insCAAACATCCAAGACACTGAGG
ENST00000372295.5:c.405-2_405-1insCAAACATCCAAGACACTGAGG ENSP00000361369.1:n.405-2_405-1insCAAACATCCAAGACACTGAGG
ENST00000372296.5:c.326-2_326-1insCAAACATCCAAGACACTGAGG ENSP00000361370.1:n.326-2_326-1insCAAACATCCAAGACACTGAGG
NM_002814.3:c.528-2_528-1insCAAACATCCAAGACACTGAGG NP_002805.1:n.528-2_528-1insCAAACATCCAAGACACTGAGG
NM_170750.2:c.449-2_449-1insCAAACATCCAAGACACTGAGG NP_736606.1:n.449-2_449-1insCAAACATCCAAGACACTGAGG
NM_002814.4:c.528-2_528-1insCAAACATCCAAGACACTGAGG MANE Select NP_002805.1:n.528-2_528-1insCAAACATCCAAGACACTGAGG
NM_170750.3:c.449-2_449-1insCAAACATCCAAGACACTGAGG NP_736606.1:n.449-2_449-1insCAAACATCCAAGACACTGAGG