Canonical Allele Identifier: CA2241308062

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810018A= , CM000678.2:g.88810018A=	GRCh38
NC_000016.9:g.88876426A= , CM000678.1:g.88876426A=	GRCh37
NC_000016.8:g.87403927A=	NCBI36
NG_008013.1:g.6917T=
NG_028266.1:g.11241A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.400+52T= MANE Select	ENSP00000367615.3:n.400+52T=
ENST00000378364.7:c.400+52T=	ENSP00000367615.3:n.400+52T=
ENST00000426324.6:c.400+52T=	ENSP00000397007.2:n.400+52T=
ENST00000562464.1:n.410+52T=
ENST00000563655.5:c.319+52T=	ENSP00000456012.1:n.319+52T=
ENST00000567057.5:n.199+52T=
ENST00000567391.5:c.*74+52T=	ENSP00000457964.1:n.*74+52T=
ENST00000567713.5:c.321+405T=	ENSP00000455749.1:n.321+405T=
ENST00000568319.5:c.*74+52T=	ENSP00000456905.1:n.*74+52T=
ENST00000568575.1:n.329+52T=
ENST00000569616.1:c.398+52T=
NM_000485.2:c.400+52T=	NP_000476.1:n.400+52T=
NM_001030018.1:c.400+52T=	NP_001025189.1:n.400+52T=
NM_000485.3:c.400+52T= MANE Select	NP_000476.1:n.400+52T=
NM_001030018.2:c.400+52T=	NP_001025189.1:n.400+52T=