Canonical Allele Identifier: CA16617329

Gene: PDE11A PDE11A-AS1

Linked Data

• ClinVar Variation Id: 422034
• ClinVar RCV Id: RCV000478741
• dbSNP Id: rs1064795513
• MyVariant Identifiers: chr2:g.178592495T>A (hg19) ; chr2:g.177727767T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177727767T>A , CM000664.2:g.177727767T>A	GRCh38
NC_000002.11:g.178592495T>A , CM000664.1:g.178592495T>A	GRCh37
NC_000002.10:g.178300741T>A	NCBI36
NG_012168.1:g.385572A>T
NG_012168.2:g.385573A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286063.11:c.1936-2A>T (PDE11A) MANE Select	ENSP00000286063.5:n.1936-2A>T
ENST00000286063.10:c.1936-2A>T (PDE11A)	ENSP00000286063.5:n.1936-2A>T
ENST00000358450.8:c.1186-2A>T (PDE11A)	ENSP00000351232.4:n.1186-2A>T
ENST00000389683.7:c.604-2A>T (PDE11A)	ENSP00000374333.3:n.604-2A>T
ENST00000409504.5:c.862-2A>T (PDE11A)	ENSP00000386539.1:n.862-2A>T
ENST00000433879.1:c.759-2A>T (PDE11A)
ENST00000497003.5:n.978-2A>T (PDE11A)
NM_001077196.1:c.604-2A>T (PDE11A)	NP_001070664.1:n.604-2A>T
NM_001077197.1:c.1186-2A>T (PDE11A)	NP_001070665.1:n.1186-2A>T
NM_001077358.1:c.862-2A>T (PDE11A)	NP_001070826.1:n.862-2A>T
NM_016953.3:c.1936-2A>T (PDE11A)	NP_058649.3:n.1936-2A>T
XM_011512284.1:c.*35-295T>A (PDE11A-AS1)	XP_011510586.1:n.*35-295T>A
NM_016953.4:c.1936-2A>T (PDE11A) MANE Select	NP_058649.3:n.1936-2A>T
NM_001077196.2:c.604-2A>T (PDE11A)	NP_001070664.1:n.604-2A>T
NM_001077197.2:c.1186-2A>T (PDE11A)	NP_001070665.1:n.1186-2A>T
NM_001077358.2:c.862-2A>T (PDE11A)	NP_001070826.1:n.862-2A>T