Canonical Allele Identifier: CA349703833
Gene: PDE11A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014368A>C , CM000664.2:g.178014368A>C GRCh38
NC_000002.11:g.178879095A>C , CM000664.1:g.178879095A>C GRCh37
NC_000002.10:g.178587341A>C NCBI36
NG_012168.1:g.98972T>G
NG_012168.2:g.98972T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286063.11:c.1005T>G MANE Select ENSP00000286063.5:p.Ile335Met
ENST00000286063.10:c.1005T>G ENSP00000286063.5:p.Ile335Met
ENST00000358450.8:c.255T>G ENSP00000351232.4:p.Ile85Met
NM_001077197.1:c.255T>G NP_001070665.1:p.Ile85Met
NM_016953.3:c.1005T>G NP_058649.3:p.Ile335Met
NM_016953.4:c.1005T>G MANE Select NP_058649.3:p.Ile335Met
NM_001077197.2:c.255T>G NP_001070665.1:p.Ile85Met