Canonical Allele Identifier: CA2577168374
Gene: PDE11A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014284A>G , CM000664.2:g.178014284A>G GRCh38
NC_000002.11:g.178879011A>G , CM000664.1:g.178879011A>G GRCh37
NC_000002.10:g.178587257A>G NCBI36
NG_012168.1:g.99056T>C
NG_012168.2:g.99056T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286063.11:c.1071+18T>C MANE Select ENSP00000286063.5:n.1071+18T>C
ENST00000286063.10:c.1071+18T>C ENSP00000286063.5:n.1071+18T>C
ENST00000358450.8:c.321+18T>C ENSP00000351232.4:n.321+18T>C
NM_001077197.1:c.321+18T>C NP_001070665.1:n.321+18T>C
NM_016953.3:c.1071+18T>C NP_058649.3:n.1071+18T>C
NM_016953.4:c.1071+18T>C MANE Select NP_058649.3:n.1071+18T>C
NM_001077197.2:c.321+18T>C NP_001070665.1:n.321+18T>C