Canonical Allele Identifier: CA400805598

Gene: PSMD12

Linked Data

• MyVariant Identifiers: chr17:g.65346436A>G (hg19) ; chr17:g.67350320A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67350320A>G , CM000679.2:g.67350320A>G	GRCh38
NC_000017.10:g.65346436A>G , CM000679.1:g.65346436A>G	GRCh37
NC_000017.9:g.62776898A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356126.8:c.314T>C MANE Select	ENSP00000348442.3:p.Val105Ala
ENST00000356126.7:c.314T>C	ENSP00000348442.3:p.Val105Ala
ENST00000357146.4:c.254T>C	ENSP00000349667.4:p.Val85Ala
ENST00000579365.5:c.*364T>C	ENSP00000463017.1:n.*364T>C
ENST00000581618.1:n.551T>C
ENST00000584008.5:c.*469T>C	ENSP00000462525.1:n.*469T>C
ENST00000584289.5:n.363T>C
NM_001316341.1:c.137T>C	NP_001303270.1:p.Val46Ala
NM_002816.3:c.314T>C	NP_002807.1:p.Val105Ala
NM_002816.4:c.314T>C	NP_002807.1:p.Val105Ala
NM_174871.2:c.254T>C	NP_777360.1:p.Val85Ala
NM_174871.3:c.254T>C	NP_777360.1:p.Val85Ala
XM_011525048.1:c.137T>C	XP_011523350.1:p.Val46Ala
XM_011525049.1:c.137T>C	XP_011523351.1:p.Val46Ala
XM_011525050.1:c.314T>C	XP_011523352.1:p.Val105Ala
XM_024450842.1:c.401T>C	XP_024306610.1:p.Val134Ala
XM_024450843.1:c.137T>C	XP_024306611.1:p.Val46Ala
XR_001752571.2:n.393T>C
NM_002816.5:c.314T>C MANE Select	NP_002807.1:p.Val105Ala
NM_001316341.2:c.137T>C	NP_001303270.1:p.Val46Ala
NM_174871.4:c.254T>C	NP_777360.1:p.Val85Ala