Canonical Allele Identifier: CA725630141

Gene: APRT

Linked Data

• dbSNP Id: rs1388337891
• MyVariant Identifiers: chr16:g.88876101T>A (hg19) ; chr16:g.88809693T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809693T>A , CM000678.2:g.88809693T>A	GRCh38
NC_000016.9:g.88876101T>A , CM000678.1:g.88876101T>A	GRCh37
NC_000016.8:g.87403602T>A	NCBI36
NG_008013.1:g.7242A>T
NG_028266.1:g.10916T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.*5A>T MANE Select	ENSP00000367615.3:n.*5A>T
ENST00000378364.7:c.*5A>T	ENSP00000367615.3:n.*5A>T
ENST00000426324.6:c.*9A>T	ENSP00000397007.2:n.*9A>T
ENST00000563655.5:c.*5A>T	ENSP00000456012.1:n.*5A>T
ENST00000567057.5:n.213A>T
ENST00000567391.5:c.*222A>T	ENSP00000457964.1:n.*222A>T
ENST00000567713.5:c.322-158A>T	ENSP00000455749.1:n.322-158A>T
ENST00000568319.5:c.*88A>T	ENSP00000456905.1:n.*88A>T
ENST00000568575.1:n.477A>T
ENST00000569616.1:c.613A>T
NM_000485.2:c.*5A>T	NP_000476.1:n.*5A>T
NM_001030018.1:c.*9A>T	NP_001025189.1:n.*9A>T
NM_000485.3:c.*5A>T MANE Select	NP_000476.1:n.*5A>T
NM_001030018.2:c.*9A>T	NP_001025189.1:n.*9A>T