Canonical Allele Identifier: CA349699640

Gene: PDE11A PDE11A-AS1

Linked Data

• MyVariant Identifiers: chr2:g.178592399A>T (hg19) ; chr2:g.177727671A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177727671A>T , CM000664.2:g.177727671A>T	GRCh38
NC_000002.11:g.178592399A>T , CM000664.1:g.178592399A>T	GRCh37
NC_000002.10:g.178300645A>T	NCBI36
NG_012168.1:g.385668T>A
NG_012168.2:g.385669T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000286063.11:c.2030T>A (PDE11A) MANE Select	ENSP00000286063.5:p.Phe677Tyr
ENST00000286063.10:c.2030T>A (PDE11A)	ENSP00000286063.5:p.Phe677Tyr
ENST00000358450.8:c.1280T>A (PDE11A)	ENSP00000351232.4:p.Phe427Tyr
ENST00000389683.7:c.698T>A (PDE11A)	ENSP00000374333.3:p.Phe233Tyr
ENST00000409504.5:c.956T>A (PDE11A)	ENSP00000386539.1:p.Phe319Tyr
ENST00000433879.1:c.853T>A (PDE11A)
ENST00000497003.5:n.1072T>A (PDE11A)
NM_001077196.1:c.698T>A (PDE11A)	NP_001070664.1:p.Phe233Tyr
NM_001077197.1:c.1280T>A (PDE11A)	NP_001070665.1:p.Phe427Tyr
NM_001077358.1:c.956T>A (PDE11A)	NP_001070826.1:p.Phe319Tyr
NM_016953.3:c.2030T>A (PDE11A)	NP_058649.3:p.Phe677Tyr
XM_011512284.1:c.*35-391A>T (PDE11A-AS1)	XP_011510586.1:n.*35-391A>T
NM_016953.4:c.2030T>A (PDE11A) MANE Select	NP_058649.3:p.Phe677Tyr
NM_001077196.2:c.698T>A (PDE11A)	NP_001070664.1:p.Phe233Tyr
NM_001077197.2:c.1280T>A (PDE11A)	NP_001070665.1:p.Phe427Tyr
NM_001077358.2:c.956T>A (PDE11A)	NP_001070826.1:p.Phe319Tyr