Canonical Allele Identifier: CA2701260597
Gene: PDE11A HGNC NCBI

Linked Data

dbSNP Id: rs2105827197
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014268A>G , CM000664.2:g.178014268A>G GRCh38
NC_000002.11:g.178878995A>G , CM000664.1:g.178878995A>G GRCh37
NC_000002.10:g.178587241A>G NCBI36
NG_012168.1:g.99072T>C
NG_012168.2:g.99072T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286063.11:c.1071+34T>C MANE Select ENSP00000286063.5:n.1071+34T>C
ENST00000286063.10:c.1071+34T>C ENSP00000286063.5:n.1071+34T>C
ENST00000358450.8:c.321+34T>C ENSP00000351232.4:n.321+34T>C
NM_001077197.1:c.321+34T>C NP_001070665.1:n.321+34T>C
NM_016953.3:c.1071+34T>C NP_058649.3:n.1071+34T>C
NM_016953.4:c.1071+34T>C MANE Select NP_058649.3:n.1071+34T>C
NM_001077197.2:c.321+34T>C NP_001070665.1:n.321+34T>C
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