Canonical Allele Identifier: CA349704034
Gene: PDE11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.178879187C>G (hg19) chr2:g.178014460C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014460C>G , CM000664.2:g.178014460C>G GRCh38
NC_000002.11:g.178879187C>G , CM000664.1:g.178879187C>G GRCh37
NC_000002.10:g.178587433C>G NCBI36
NG_012168.1:g.98880G>C
NG_012168.2:g.98880G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286063.11:c.913G>C MANE Select ENSP00000286063.5:p.Asp305His
ENST00000286063.10:c.913G>C ENSP00000286063.5:p.Asp305His
ENST00000358450.8:c.163G>C ENSP00000351232.4:p.Asp55His
NM_001077197.1:c.163G>C NP_001070665.1:p.Asp55His
NM_016953.3:c.913G>C NP_058649.3:p.Asp305His
NM_016953.4:c.913G>C MANE Select NP_058649.3:p.Asp305His
NM_001077197.2:c.163G>C NP_001070665.1:p.Asp55His
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