Canonical Allele Identifier: CA517921638

Gene: PSMD10 ATG4A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108091512C>A , CM000685.2:g.108091512C>A	GRCh38
NC_000023.10:g.107334742C>A , CM000685.1:g.107334742C>A	GRCh37
NC_000023.9:g.107221398C>A	NCBI36
NG_012521.1:g.5107G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002814.4:c.9G>T (PSMD10) MANE Select	NP_002805.1:p.Gly3=
ENST00000217958.8:c.9G>T (PSMD10) MANE Select	ENSP00000217958.3:p.Gly3=
NM_002814.3:c.9G>T (PSMD10)	NP_002805.1:p.Gly3=
NM_170750.2:c.9G>T (PSMD10)	NP_736606.1:p.Gly3=
NM_170750.3:c.9G>T (PSMD10)	NP_736606.1:p.Gly3=
ENST00000217958.7:c.9G>T (PSMD10)	ENSP00000217958.3:p.Gly3=
ENST00000338548.4:n.38G>T (PSMD10)
ENST00000340200.5:c.9G>T (PSMD10)	ENSP00000345963.5:p.Gly3=
ENST00000361815.9:c.9G>T (PSMD10)	ENSP00000354906.5:p.Gly3=
ENST00000372295.5:c.9G>T (PSMD10)	ENSP00000361369.1:p.Gly3=
ENST00000372296.5:c.9G>T (PSMD10)	ENSP00000361370.1:p.Gly3=
ENST00000553388.1:n.27G>T (PSMD10)
XM_011530840.1:c.22+2542C>A (ATG4A)	XP_011529142.1:n.22+2542C>A
XM_011530841.1:c.22+2542C>A (ATG4A)	XP_011529143.1:n.22+2542C>A