Canonical Allele Identifier: CA2241307812

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809646C= , CM000678.2:g.88809646C=	GRCh38
NC_000016.9:g.88876054C= , CM000678.1:g.88876054C=	GRCh37
NC_000016.8:g.87403555C=	NCBI36
NG_008013.1:g.7289G=
NG_028266.1:g.10869C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.*52G= MANE Select	ENSP00000367615.3:n.*52G=
ENST00000378364.7:c.*52G=	ENSP00000367615.3:n.*52G=
ENST00000426324.6:c.*56G=	ENSP00000397007.2:n.*56G=
ENST00000563655.5:c.*52G=	ENSP00000456012.1:n.*52G=
ENST00000567057.5:n.260G=
ENST00000567391.5:c.*269G=	ENSP00000457964.1:n.*269G=
ENST00000567713.5:c.322-111G=	ENSP00000455749.1:n.322-111G=
ENST00000568319.5:c.*135G=	ENSP00000456905.1:n.*135G=
ENST00000569616.1:c.660G=
NM_000485.2:c.*52G=	NP_000476.1:n.*52G=
NM_001030018.1:c.*56G=	NP_001025189.1:n.*56G=
NM_000485.3:c.*52G= MANE Select	NP_000476.1:n.*52G=
NM_001030018.2:c.*56G=	NP_001025189.1:n.*56G=