Canonical Allele Identifier: CA1946989630

Gene: PSMD13

Genomic Alleles

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

Transcript Alleles

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