Canonical Allele Identifier: CA2241308145

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810133G= , CM000678.2:g.88810133G=	GRCh38
NC_000016.9:g.88876541G= , CM000678.1:g.88876541G=	GRCh37
NC_000016.8:g.87404042G=	NCBI36
NG_008013.1:g.6802C=
NG_028266.1:g.11356G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.337C= MANE Select	ENSP00000367615.3:p.Gln113=
ENST00000378364.7:c.337C=	ENSP00000367615.3:p.Gln113=
ENST00000426324.6:c.337C=	ENSP00000397007.2:p.Gln113=
ENST00000562464.1:n.347C=
ENST00000563655.5:c.256C=	ENSP00000456012.1:p.Gln86=
ENST00000567057.5:n.136C=
ENST00000567391.5:c.*11C=	ENSP00000457964.1:n.*11C=
ENST00000567713.5:c.321+290C=	ENSP00000455749.1:n.321+290C=
ENST00000568319.5:c.*11C=	ENSP00000456905.1:n.*11C=
ENST00000568575.1:n.266C=
ENST00000569616.1:c.335C=
NM_000485.2:c.337C=	NP_000476.1:p.Gln113=
NM_001030018.1:c.337C=	NP_001025189.1:p.Gln113=
NM_000485.3:c.337C= MANE Select	NP_000476.1:p.Gln113=
NM_001030018.2:c.337C=	NP_001025189.1:p.Gln113=