Canonical Allele Identifier: CA2450520139

Gene: PSMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084347C= , CM000685.2:g.108084347C=	GRCh38
NC_000023.10:g.107327577C= , CM000685.1:g.107327577C=	GRCh37
NC_000023.9:g.107214233C=	NCBI36
NG_012521.1:g.12272G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*627G= MANE Select	ENSP00000217958.3:n.*627G=
ENST00000217958.7:c.*627G=	ENSP00000217958.3:n.*627G=
NM_002814.3:c.*627G=	NP_002805.1:n.*627G=
NM_170750.2:c.*773G=	NP_736606.1:n.*773G=
NM_002814.4:c.*627G= MANE Select	NP_002805.1:n.*627G=
NM_170750.3:c.*773G=	NP_736606.1:n.*773G=