Canonical Allele Identifier: CA16617329
Gene: PDE11A HGNC NCBI
PDE11A-AS1 HGNC NCBI

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)
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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
Search 100 bp 5'
Search 100 bp 3'