Canonical Allele Identifier: CA400805469

Gene: PSMD12

Linked Data

• MyVariant Identifiers: chr17:g.65346378T>A (hg19) ; chr17:g.67350262T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67350262T>A , CM000679.2:g.67350262T>A	GRCh38
NC_000017.10:g.65346378T>A , CM000679.1:g.65346378T>A	GRCh37
NC_000017.9:g.62776840T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356126.8:c.372A>T MANE Select	ENSP00000348442.3:p.Leu124Phe
ENST00000356126.7:c.372A>T	ENSP00000348442.3:p.Leu124Phe
ENST00000357146.4:c.312A>T	ENSP00000349667.4:p.Leu104Phe
ENST00000581618.1:n.609A>T
ENST00000584008.5:c.*527A>T	ENSP00000462525.1:n.*527A>T
ENST00000584289.5:n.421A>T
NM_001316341.1:c.195A>T	NP_001303270.1:p.Leu65Phe
NM_002816.3:c.372A>T	NP_002807.1:p.Leu124Phe
NM_002816.4:c.372A>T	NP_002807.1:p.Leu124Phe
NM_174871.2:c.312A>T	NP_777360.1:p.Leu104Phe
NM_174871.3:c.312A>T	NP_777360.1:p.Leu104Phe
XM_011525048.1:c.195A>T	XP_011523350.1:p.Leu65Phe
XM_011525049.1:c.195A>T	XP_011523351.1:p.Leu65Phe
XM_011525050.1:c.372A>T	XP_011523352.1:p.Leu124Phe
XM_024450842.1:c.459A>T	XP_024306610.1:p.Leu153Phe
XM_024450843.1:c.195A>T	XP_024306611.1:p.Leu65Phe
XR_001752571.2:n.451A>T
NM_002816.5:c.372A>T MANE Select	NP_002807.1:p.Leu124Phe
NM_001316341.2:c.195A>T	NP_001303270.1:p.Leu65Phe
NM_174871.4:c.312A>T	NP_777360.1:p.Leu104Phe