Canonical Allele Identifier: CA8234436

Gene: APRT

Linked Data

• dbSNP Id: rs542789654
• ExAC: 16:88876512 C / T
• gnomAD v4: 16-88810104-C-T
• MyVariant Identifiers: chr16:g.88876512C>T (hg19) ; chr16:g.88810104C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810104C>T , CM000678.2:g.88810104C>T	GRCh38
NC_000016.9:g.88876512C>T , CM000678.1:g.88876512C>T	GRCh37
NC_000016.8:g.87404013C>T	NCBI36
NG_008013.1:g.6831G>A
NG_028266.1:g.11327C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.366G>A MANE Select	ENSP00000367615.3:p.Arg122=
ENST00000378364.7:c.366G>A	ENSP00000367615.3:p.Arg122=
ENST00000426324.6:c.366G>A	ENSP00000397007.2:p.Arg122=
ENST00000562464.1:n.376G>A
ENST00000563655.5:c.285G>A	ENSP00000456012.1:p.Arg95=
ENST00000567057.5:n.165G>A
ENST00000567391.5:c.*40G>A	ENSP00000457964.1:n.*40G>A
ENST00000567713.5:c.321+319G>A	ENSP00000455749.1:n.321+319G>A
ENST00000568319.5:c.*40G>A	ENSP00000456905.1:n.*40G>A
ENST00000568575.1:n.295G>A
ENST00000569616.1:c.364G>A
NM_000485.2:c.366G>A	NP_000476.1:p.Arg122=
NM_001030018.1:c.366G>A	NP_001025189.1:p.Arg122=
NM_000485.3:c.366G>A MANE Select	NP_000476.1:p.Arg122=
NM_001030018.2:c.366G>A	NP_001025189.1:p.Arg122=