Canonical Allele Identifier: CA349703690

Gene: PDE11A

Linked Data

• MyVariant Identifiers: chr2:g.178879031T>A (hg19) ; chr2:g.178014304T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178014304T>A , CM000664.2:g.178014304T>A	GRCh38
NC_000002.11:g.178879031T>A , CM000664.1:g.178879031T>A	GRCh37
NC_000002.10:g.178587277T>A	NCBI36
NG_012168.1:g.99036A>T
NG_012168.2:g.99036A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286063.11:c.1069A>T MANE Select	ENSP00000286063.5:p.Lys357Ter
ENST00000286063.10:c.1069A>T	ENSP00000286063.5:p.Lys357Ter
ENST00000358450.8:c.319A>T	ENSP00000351232.4:p.Lys107Ter
NM_001077197.1:c.319A>T	NP_001070665.1:p.Lys107Ter
NM_016953.3:c.1069A>T	NP_058649.3:p.Lys357Ter
NM_016953.4:c.1069A>T MANE Select	NP_058649.3:p.Lys357Ter
NM_001077197.2:c.319A>T	NP_001070665.1:p.Lys107Ter