Canonical Allele Identifier: CA2241307816

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809653T= , CM000678.2:g.88809653T=	GRCh38
NC_000016.9:g.88876061T= , CM000678.1:g.88876061T=	GRCh37
NC_000016.8:g.87403562T=	NCBI36
NG_008013.1:g.7282A=
NG_028266.1:g.10876T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.*45A= MANE Select	ENSP00000367615.3:n.*45A=
ENST00000378364.7:c.*45A=	ENSP00000367615.3:n.*45A=
ENST00000426324.6:c.*49A=	ENSP00000397007.2:n.*49A=
ENST00000563655.5:c.*45A=	ENSP00000456012.1:n.*45A=
ENST00000567057.5:n.253A=
ENST00000567391.5:c.*262A=	ENSP00000457964.1:n.*262A=
ENST00000567713.5:c.322-118A=	ENSP00000455749.1:n.322-118A=
ENST00000568319.5:c.*128A=	ENSP00000456905.1:n.*128A=
ENST00000569616.1:c.653A=
NM_000485.2:c.*45A=	NP_000476.1:n.*45A=
NM_001030018.1:c.*49A=	NP_001025189.1:n.*49A=
NM_000485.3:c.*45A= MANE Select	NP_000476.1:n.*45A=
NM_001030018.2:c.*49A=	NP_001025189.1:n.*49A=