Canonical Allele Identifier: CA2241307832

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809683T= , CM000678.2:g.88809683T=	GRCh38
NC_000016.9:g.88876091T= , CM000678.1:g.88876091T=	GRCh37
NC_000016.8:g.87403592T=	NCBI36
NG_008013.1:g.7252A=
NG_028266.1:g.10906T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.*15A= MANE Select	ENSP00000367615.3:n.*15A=
ENST00000378364.7:c.*15A=	ENSP00000367615.3:n.*15A=
ENST00000426324.6:c.*19A=	ENSP00000397007.2:n.*19A=
ENST00000563655.5:c.*15A=	ENSP00000456012.1:n.*15A=
ENST00000567057.5:n.223A=
ENST00000567391.5:c.*232A=	ENSP00000457964.1:n.*232A=
ENST00000567713.5:c.322-148A=	ENSP00000455749.1:n.322-148A=
ENST00000568319.5:c.*98A=	ENSP00000456905.1:n.*98A=
ENST00000568575.1:n.487A=
ENST00000569616.1:c.623A=
NM_000485.2:c.*15A=	NP_000476.1:n.*15A=
NM_001030018.1:c.*19A=	NP_001025189.1:n.*19A=
NM_000485.3:c.*15A= MANE Select	NP_000476.1:n.*15A=
NM_001030018.2:c.*19A=	NP_001025189.1:n.*19A=