Canonical Allele Identifier: CA2450520141

Gene: PSMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084351C= , CM000685.2:g.108084351C=	GRCh38
NC_000023.10:g.107327581C= , CM000685.1:g.107327581C=	GRCh37
NC_000023.9:g.107214237C=	NCBI36
NG_012521.1:g.12268G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*623G= MANE Select	ENSP00000217958.3:n.*623G=
ENST00000217958.7:c.*623G=	ENSP00000217958.3:n.*623G=
NM_002814.3:c.*623G=	NP_002805.1:n.*623G=
NM_170750.2:c.*769G=	NP_736606.1:n.*769G=
NM_002814.4:c.*623G= MANE Select	NP_002805.1:n.*623G=
NM_170750.3:c.*769G=	NP_736606.1:n.*769G=