Canonical Allele Identifier: CA349703815
Gene: PDE11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.178879087A>G (hg19) chr2:g.178014360A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014360A>G , CM000664.2:g.178014360A>G GRCh38
NC_000002.11:g.178879087A>G , CM000664.1:g.178879087A>G GRCh37
NC_000002.10:g.178587333A>G NCBI36
NG_012168.1:g.98980T>C
NG_012168.2:g.98980T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000286063.11:c.1013T>C MANE Select ENSP00000286063.5:p.Val338Ala
ENST00000286063.10:c.1013T>C ENSP00000286063.5:p.Val338Ala
ENST00000358450.8:c.263T>C ENSP00000351232.4:p.Val88Ala
NM_001077197.1:c.263T>C NP_001070665.1:p.Val88Ala
NM_016953.3:c.1013T>C NP_058649.3:p.Val338Ala
NM_016953.4:c.1013T>C MANE Select NP_058649.3:p.Val338Ala
NM_001077197.2:c.263T>C NP_001070665.1:p.Val88Ala
Search 100 bp 5'
Search 100 bp 3'