Canonical Allele Identifier: CA397091296

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88811842G>A , CM000678.2:g.88811842G>A	GRCh38
NC_000016.9:g.88878250G>A , CM000678.1:g.88878250G>A	GRCh37
NC_000016.8:g.87405751G>A	NCBI36
NG_008013.1:g.5093C>T
NG_008667.1:g.50125C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000485.3:c.58C>T MANE Select	NP_000476.1:p.Pro20Ser
ENST00000378364.8:c.58C>T MANE Select	ENSP00000367615.3:p.Pro20Ser
NM_000485.2:c.58C>T	NP_000476.1:p.Pro20Ser
NM_001030018.1:c.58C>T	NP_001025189.1:p.Pro20Ser
NM_001030018.2:c.58C>T	NP_001025189.1:p.Pro20Ser
ENST00000378364.7:c.58C>T	ENSP00000367615.3:p.Pro20Ser
ENST00000426324.6:c.58C>T	ENSP00000397007.2:p.Pro20Ser
ENST00000562464.1:n.39C>T
ENST00000563655.5:c.58C>T	ENSP00000456012.1:p.Pro20Ser
ENST00000564858.1:n.79C>T
ENST00000567391.5:c.58C>T	ENSP00000457964.1:p.Pro20Ser
ENST00000567713.5:c.58C>T	ENSP00000455749.1:p.Pro20Ser
ENST00000568319.5:c.58C>T	ENSP00000456905.1:p.Pro20Ser
ENST00000569616.1:c.56C>T