Canonical Allele Identifier: CA2241307847

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809700A= , CM000678.2:g.88809700A=	GRCh38
NC_000016.9:g.88876108A= , CM000678.1:g.88876108A=	GRCh37
NC_000016.8:g.87403609A=	NCBI36
NG_008013.1:g.7235T=
NG_028266.1:g.10923A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.541T= MANE Select	ENSP00000367615.3:p.Ter181=
ENST00000378364.7:c.541T=	ENSP00000367615.3:p.Ter181=
ENST00000426324.6:c.*2T=	ENSP00000397007.2:n.*2T=
ENST00000563655.5:c.460T=	ENSP00000456012.1:p.Ter154=
ENST00000567057.5:n.206T=
ENST00000567391.5:c.*215T=	ENSP00000457964.1:n.*215T=
ENST00000567713.5:c.322-165T=	ENSP00000455749.1:n.322-165T=
ENST00000568319.5:c.*81T=	ENSP00000456905.1:n.*81T=
ENST00000568575.1:n.470T=
ENST00000569616.1:c.606T=
NM_000485.2:c.541T=	NP_000476.1:p.Ter181=
NM_001030018.1:c.*2T=	NP_001025189.1:n.*2T=
NM_000485.3:c.541T= MANE Select	NP_000476.1:p.Ter181=
NM_001030018.2:c.*2T=	NP_001025189.1:n.*2T=