Canonical Allele Identifier: CA349703811
Gene: PDE11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.178879085C>A (hg19) chr2:g.178014358C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014358C>A , CM000664.2:g.178014358C>A GRCh38
NC_000002.11:g.178879085C>A , CM000664.1:g.178879085C>A GRCh37
NC_000002.10:g.178587331C>A NCBI36
NG_012168.1:g.98982G>T
NG_012168.2:g.98982G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000286063.11:c.1015G>T MANE Select ENSP00000286063.5:p.Ala339Ser
ENST00000286063.10:c.1015G>T ENSP00000286063.5:p.Ala339Ser
ENST00000358450.8:c.265G>T ENSP00000351232.4:p.Ala89Ser
NM_001077197.1:c.265G>T NP_001070665.1:p.Ala89Ser
NM_016953.3:c.1015G>T NP_058649.3:p.Ala339Ser
NM_016953.4:c.1015G>T MANE Select NP_058649.3:p.Ala339Ser
NM_001077197.2:c.265G>T NP_001070665.1:p.Ala89Ser
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