Canonical Allele Identifier: CA1136170266

Gene: PSMD10

Linked Data

• dbSNP Id: rs2031479744
• gnomAD v3: X-108085018-TG-T
• gnomAD v4: X-108085018-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085020del , CM000685.2:g.108085020del	GRCh38
NC_000023.10:g.107328250del , CM000685.1:g.107328250del	GRCh37
NC_000023.9:g.107214906del	NCBI36
NG_012521.1:g.11600del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.636del MANE Select	ENSP00000217958.3:p.Gly214ValfsTer5
ENST00000217958.7:c.636del	ENSP00000217958.3:p.Gly214ValfsTer5
ENST00000340200.5:c.537del	ENSP00000345963.5:p.Gly181ValfsTer5
ENST00000361815.9:c.*101del	ENSP00000354906.5:n.*101del
ENST00000372295.5:c.513del	ENSP00000361369.1:p.Gly173ValfsTer5
ENST00000372296.5:c.*101del	ENSP00000361370.1:n.*101del
NM_002814.3:c.636del	NP_002805.1:p.Gly214ValfsTer5
NM_170750.2:c.*101del	NP_736606.1:n.*101del
NM_002814.4:c.636del MANE Select	NP_002805.1:p.Gly214ValfsTer5
NM_170750.3:c.*101del	NP_736606.1:n.*101del