Canonical Allele Identifier: CA2241308395

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810486G= , CM000678.2:g.88810486G=	GRCh38
NC_000016.9:g.88876894G= , CM000678.1:g.88876894G=	GRCh37
NC_000016.8:g.87404395G=	NCBI36
NG_008013.1:g.6449C=
NG_028266.1:g.11709G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.258C= MANE Select	ENSP00000367615.3:p.Ile86=
ENST00000378364.7:c.258C=	ENSP00000367615.3:p.Ile86=
ENST00000426324.6:c.258C=	ENSP00000397007.2:p.Ile86=
ENST00000562464.1:n.332-338C=
ENST00000563655.5:c.241-338C=	ENSP00000456012.1:n.241-338C=
ENST00000567391.5:c.188-338C=	ENSP00000457964.1:n.188-338C=
ENST00000567713.5:c.258C=	ENSP00000455749.1:p.Ile86=
ENST00000568319.5:c.188-338C=	ENSP00000456905.1:n.188-338C=
ENST00000569616.1:c.256C=
NM_000485.2:c.258C=	NP_000476.1:p.Ile86=
NM_001030018.1:c.258C=	NP_001025189.1:p.Ile86=
NM_000485.3:c.258C= MANE Select	NP_000476.1:p.Ile86=
NM_001030018.2:c.258C=	NP_001025189.1:p.Ile86=