Canonical Allele Identifier: CA349703822
Gene: PDE11A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014363C>G , CM000664.2:g.178014363C>G GRCh38
NC_000002.11:g.178879090C>G , CM000664.1:g.178879090C>G GRCh37
NC_000002.10:g.178587336C>G NCBI36
NG_012168.1:g.98977G>C
NG_012168.2:g.98977G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000286063.11:c.1010G>C MANE Select ENSP00000286063.5:p.Gly337Ala
ENST00000286063.10:c.1010G>C ENSP00000286063.5:p.Gly337Ala
ENST00000358450.8:c.260G>C ENSP00000351232.4:p.Gly87Ala
NM_001077197.1:c.260G>C NP_001070665.1:p.Gly87Ala
NM_016953.3:c.1010G>C NP_058649.3:p.Gly337Ala
NM_016953.4:c.1010G>C MANE Select NP_058649.3:p.Gly337Ala
NM_001077197.2:c.260G>C NP_001070665.1:p.Gly87Ala