Canonical Allele Identifier: CA400805602

Gene: PSMD12

Linked Data

• MyVariant Identifiers: chr17:g.65346437C>T (hg19) ; chr17:g.67350321C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67350321C>T , CM000679.2:g.67350321C>T	GRCh38
NC_000017.10:g.65346437C>T , CM000679.1:g.65346437C>T	GRCh37
NC_000017.9:g.62776899C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356126.8:c.313G>A MANE Select	ENSP00000348442.3:p.Val105Ile
ENST00000356126.7:c.313G>A	ENSP00000348442.3:p.Val105Ile
ENST00000357146.4:c.253G>A	ENSP00000349667.4:p.Val85Ile
ENST00000579365.5:c.*363G>A	ENSP00000463017.1:n.*363G>A
ENST00000581618.1:n.550G>A
ENST00000584008.5:c.*468G>A	ENSP00000462525.1:n.*468G>A
ENST00000584289.5:n.362G>A
NM_001316341.1:c.136G>A	NP_001303270.1:p.Val46Ile
NM_002816.3:c.313G>A	NP_002807.1:p.Val105Ile
NM_002816.4:c.313G>A	NP_002807.1:p.Val105Ile
NM_174871.2:c.253G>A	NP_777360.1:p.Val85Ile
NM_174871.3:c.253G>A	NP_777360.1:p.Val85Ile
XM_011525048.1:c.136G>A	XP_011523350.1:p.Val46Ile
XM_011525049.1:c.136G>A	XP_011523351.1:p.Val46Ile
XM_011525050.1:c.313G>A	XP_011523352.1:p.Val105Ile
XM_024450842.1:c.400G>A	XP_024306610.1:p.Val134Ile
XM_024450843.1:c.136G>A	XP_024306611.1:p.Val46Ile
XR_001752571.2:n.392G>A
NM_002816.5:c.313G>A MANE Select	NP_002807.1:p.Val105Ile
NM_001316341.2:c.136G>A	NP_001303270.1:p.Val46Ile
NM_174871.4:c.253G>A	NP_777360.1:p.Val85Ile