Canonical Allele Identifier: CA2241308447

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810560T= , CM000678.2:g.88810560T=	GRCh38
NC_000016.9:g.88876968T= , CM000678.1:g.88876968T=	GRCh37
NC_000016.8:g.87404469T=	NCBI36
NG_008013.1:g.6375A=
NG_028266.1:g.11783T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.188-4A= MANE Select	ENSP00000367615.3:n.188-4A=
ENST00000378364.7:c.188-4A=	ENSP00000367615.3:n.188-4A=
ENST00000426324.6:c.188-4A=	ENSP00000397007.2:n.188-4A=
ENST00000562464.1:n.332-412A=
ENST00000563655.5:c.241-412A=	ENSP00000456012.1:n.241-412A=
ENST00000567391.5:c.188-412A=	ENSP00000457964.1:n.188-412A=
ENST00000567713.5:c.188-4A=	ENSP00000455749.1:n.188-4A=
ENST00000568319.5:c.188-412A=	ENSP00000456905.1:n.188-412A=
ENST00000569616.1:c.186-4A=
NM_000485.2:c.188-4A=	NP_000476.1:n.188-4A=
NM_001030018.1:c.188-4A=	NP_001025189.1:n.188-4A=
NM_000485.3:c.188-4A= MANE Select	NP_000476.1:n.188-4A=
NM_001030018.2:c.188-4A=	NP_001025189.1:n.188-4A=