Canonical Allele Identifier: CA2241308091

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810053T= , CM000678.2:g.88810053T=	GRCh38
NC_000016.9:g.88876461T= , CM000678.1:g.88876461T=	GRCh37
NC_000016.8:g.87403962T=	NCBI36
NG_008013.1:g.6882A=
NG_028266.1:g.11276T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378364.8:c.400+17A= MANE Select	ENSP00000367615.3:n.400+17A=
ENST00000378364.7:c.400+17A=	ENSP00000367615.3:n.400+17A=
ENST00000426324.6:c.400+17A=	ENSP00000397007.2:n.400+17A=
ENST00000562464.1:n.410+17A=
ENST00000563655.5:c.319+17A=	ENSP00000456012.1:n.319+17A=
ENST00000567057.5:n.199+17A=
ENST00000567391.5:c.*74+17A=	ENSP00000457964.1:n.*74+17A=
ENST00000567713.5:c.321+370A=	ENSP00000455749.1:n.321+370A=
ENST00000568319.5:c.*74+17A=	ENSP00000456905.1:n.*74+17A=
ENST00000568575.1:n.329+17A=
ENST00000569616.1:c.398+17A=
NM_000485.2:c.400+17A=	NP_000476.1:n.400+17A=
NM_001030018.1:c.400+17A=	NP_001025189.1:n.400+17A=
NM_000485.3:c.400+17A= MANE Select	NP_000476.1:n.400+17A=
NM_001030018.2:c.400+17A=	NP_001025189.1:n.400+17A=