Canonical Allele Identifier: CA349703821
Gene: PDE11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.178879090C>A (hg19) chr2:g.178014363C>A (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000286063.11:c.1010G>T MANE Select ENSP00000286063.5:p.Gly337Val
ENST00000286063.10:c.1010G>T ENSP00000286063.5:p.Gly337Val
ENST00000358450.8:c.260G>T ENSP00000351232.4:p.Gly87Val
NM_001077197.1:c.260G>T NP_001070665.1:p.Gly87Val
NM_016953.3:c.1010G>T NP_058649.3:p.Gly337Val
NM_016953.4:c.1010G>T MANE Select NP_058649.3:p.Gly337Val
NM_001077197.2:c.260G>T NP_001070665.1:p.Gly87Val
Search 100 bp 5'
Search 100 bp 3'