Canonical Allele Identifier: CA430205428

Gene: PDE11A

Linked Data

• MyVariant Identifiers: chr2:g.178879068C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178014341C>T , CM000664.2:g.178014341C>T	GRCh38
NC_000002.11:g.178879068C>T , CM000664.1:g.178879068C>T	GRCh37
NC_000002.10:g.178587314C>T	NCBI36
NG_012168.1:g.98999G>A
NG_012168.2:g.98999G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286063.11:c.1032G>A MANE Select	ENSP00000286063.5:p.Lys344=
ENST00000286063.10:c.1032G>A	ENSP00000286063.5:p.Lys344=
ENST00000358450.8:c.282G>A	ENSP00000351232.4:p.Lys94=
NM_001077197.1:c.282G>A	NP_001070665.1:p.Lys94=
NM_016953.3:c.1032G>A	NP_058649.3:p.Lys344=
NM_016953.4:c.1032G>A MANE Select	NP_058649.3:p.Lys344=
NM_001077197.2:c.282G>A	NP_001070665.1:p.Lys94=