Canonical Allele Identifier: CA2450520324

Gene: PSMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085018T= , CM000685.2:g.108085018T=	GRCh38
NC_000023.10:g.107328248T= , CM000685.1:g.107328248T=	GRCh37
NC_000023.9:g.107214904T=	NCBI36
NG_012521.1:g.11601A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.637A= MANE Select	ENSP00000217958.3:p.Lys213=
ENST00000217958.7:c.637A=	ENSP00000217958.3:p.Lys213=
ENST00000340200.5:c.538A=	ENSP00000345963.5:p.Lys180=
ENST00000361815.9:c.*102A=	ENSP00000354906.5:n.*102A=
ENST00000372295.5:c.514A=	ENSP00000361369.1:p.Lys172=
ENST00000372296.5:c.*102A=	ENSP00000361370.1:n.*102A=
NM_002814.3:c.637A=	NP_002805.1:p.Lys213=
NM_170750.2:c.*102A=	NP_736606.1:n.*102A=
NM_002814.4:c.637A= MANE Select	NP_002805.1:p.Lys213=
NM_170750.3:c.*102A=	NP_736606.1:n.*102A=