Canonical Allele Identifier: CA1310160755

Gene: PDE11A PDE11A-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177727673C= , CM000664.2:g.177727673C=	GRCh38
NC_000002.11:g.178592401C= , CM000664.1:g.178592401C=	GRCh37
NC_000002.10:g.178300647C=	NCBI36
NG_012168.1:g.385666G=
NG_012168.2:g.385667G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000286063.11:c.2028G= (PDE11A) MANE Select	ENSP00000286063.5:p.Met676=
ENST00000286063.10:c.2028G= (PDE11A)	ENSP00000286063.5:p.Met676=
ENST00000358450.8:c.1278G= (PDE11A)	ENSP00000351232.4:p.Met426=
ENST00000389683.7:c.696G= (PDE11A)	ENSP00000374333.3:p.Met232=
ENST00000409504.5:c.954G= (PDE11A)	ENSP00000386539.1:p.Met318=
ENST00000433879.1:c.851G= (PDE11A)
ENST00000497003.5:n.1070G= (PDE11A)
NM_001077196.1:c.696G= (PDE11A)	NP_001070664.1:p.Met232=
NM_001077197.1:c.1278G= (PDE11A)	NP_001070665.1:p.Met426=
NM_001077358.1:c.954G= (PDE11A)	NP_001070826.1:p.Met318=
NM_016953.3:c.2028G= (PDE11A)	NP_058649.3:p.Met676=
XM_011512284.1:c.*35-389C= (PDE11A-AS1)	XP_011510586.1:n.*35-389C=
NM_016953.4:c.2028G= (PDE11A) MANE Select	NP_058649.3:p.Met676=
NM_001077196.2:c.696G= (PDE11A)	NP_001070664.1:p.Met232=
NM_001077197.2:c.1278G= (PDE11A)	NP_001070665.1:p.Met426=
NM_001077358.2:c.954G= (PDE11A)	NP_001070826.1:p.Met318=