Canonical Allele Identifier: CA725630114

Gene: APRT

Linked Data

• dbSNP Id: rs769454426
• gnomAD v3: 16-88809666-A-C
• gnomAD v4: 16-88809666-A-C
• MyVariant Identifiers: chr16:g.88876074A>C (hg19) ; chr16:g.88809666A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809666A>C , CM000678.2:g.88809666A>C	GRCh38
NC_000016.9:g.88876074A>C , CM000678.1:g.88876074A>C	GRCh37
NC_000016.8:g.87403575A>C	NCBI36
NG_008013.1:g.7269T>G
NG_028266.1:g.10889A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.*32T>G MANE Select	ENSP00000367615.3:n.*32T>G
ENST00000378364.7:c.*32T>G	ENSP00000367615.3:n.*32T>G
ENST00000426324.6:c.*36T>G	ENSP00000397007.2:n.*36T>G
ENST00000563655.5:c.*32T>G	ENSP00000456012.1:n.*32T>G
ENST00000567057.5:n.240T>G
ENST00000567391.5:c.*249T>G	ENSP00000457964.1:n.*249T>G
ENST00000567713.5:c.322-131T>G	ENSP00000455749.1:n.322-131T>G
ENST00000568319.5:c.*115T>G	ENSP00000456905.1:n.*115T>G
ENST00000569616.1:c.640T>G
NM_000485.2:c.*32T>G	NP_000476.1:n.*32T>G
NM_001030018.1:c.*36T>G	NP_001025189.1:n.*36T>G
NM_000485.3:c.*32T>G MANE Select	NP_000476.1:n.*32T>G
NM_001030018.2:c.*36T>G	NP_001025189.1:n.*36T>G