Canonical Allele Identifier: CA13453037
Gene: PSMD13 HGNC NCBI

Linked Data

dbSNP Id: rs505404
gnomAD v2: 11-243268-T-G
gnomAD v3: 11-243268-T-G
gnomAD v4: 11-243268-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.243268T>G , CM000673.2:g.243268T>G GRCh38
NC_000011.9:g.243268T>G , CM000673.1:g.243268T>G GRCh37
NC_000011.8:g.233268T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000532097.6:c.175-773T>G MANE Select ENSP00000436186.1:n.175-773T>G
ENST00000352303.9:c.175-773T>G ENSP00000333811.5:n.175-773T>G
ENST00000382671.8:c.175-893T>G ENSP00000372117.4:n.175-893T>G
ENST00000431206.6:c.96-773T>G ENSP00000396937.2:n.96-773T>G
ENST00000525665.5:c.175-773T>G ENSP00000434587.1:n.175-773T>G
ENST00000527047.5:n.142-773T>G
ENST00000528906.5:c.96-893T>G ENSP00000433364.1:n.96-893T>G
ENST00000529372.5:c.175-773T>G ENSP00000436795.1:n.175-773T>G
ENST00000532097.5:c.175-773T>G ENSP00000436186.1:n.175-773T>G
ENST00000534590.5:n.248-773T>G
ENST00000620253.1:n.216A>C
ENST00000621534.4:c.175-773T>G ENSP00000478756.1:n.175-773T>G
NM_002817.3:c.175-773T>G NP_002808.3:n.175-773T>G
NM_175932.2:c.96-773T>G NP_787128.2:n.96-773T>G
XM_011520235.1:c.175-773T>G XP_011518537.1:n.175-773T>G
XM_011520235.3:c.175-773T>G XP_011518537.1:n.175-773T>G
NM_002817.4:c.175-773T>G MANE Select NP_002808.3:n.175-773T>G
NM_175932.3:c.96-773T>G NP_787128.2:n.96-773T>G