Canonical Allele Identifier: CA2241308105

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810073C= , CM000678.2:g.88810073C=	GRCh38
NC_000016.9:g.88876481C= , CM000678.1:g.88876481C=	GRCh37
NC_000016.8:g.87403982C=	NCBI36
NG_008013.1:g.6862G=
NG_028266.1:g.11296C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.397G= MANE Select	ENSP00000367615.3:p.Gly133=
ENST00000378364.7:c.397G=	ENSP00000367615.3:p.Gly133=
ENST00000426324.6:c.397G=	ENSP00000397007.2:p.Gly133=
ENST00000562464.1:n.407G=
ENST00000563655.5:c.316G=	ENSP00000456012.1:p.Gly106=
ENST00000567057.5:n.196G=
ENST00000567391.5:c.*71G=	ENSP00000457964.1:n.*71G=
ENST00000567713.5:c.321+350G=	ENSP00000455749.1:n.321+350G=
ENST00000568319.5:c.*71G=	ENSP00000456905.1:n.*71G=
ENST00000568575.1:n.326G=
ENST00000569616.1:c.395G=
NM_000485.2:c.397G=	NP_000476.1:p.Gly133=
NM_001030018.1:c.397G=	NP_001025189.1:p.Gly133=
NM_000485.3:c.397G= MANE Select	NP_000476.1:p.Gly133=
NM_001030018.2:c.397G=	NP_001025189.1:p.Gly133=