Canonical Allele Identifier: CA397088368

Gene: APRT

Linked Data

• gnomAD v4: 16-88810467-G-T
• MyVariant Identifiers: chr16:g.88876875G>T (hg19) ; chr16:g.88810467G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810467G>T , CM000678.2:g.88810467G>T	GRCh38
NC_000016.9:g.88876875G>T , CM000678.1:g.88876875G>T	GRCh37
NC_000016.8:g.87404376G>T	NCBI36
NG_008013.1:g.6468C>A
NG_028266.1:g.11690G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.277C>A MANE Select	ENSP00000367615.3:p.Pro93Thr
ENST00000378364.7:c.277C>A	ENSP00000367615.3:p.Pro93Thr
ENST00000426324.6:c.277C>A	ENSP00000397007.2:p.Pro93Thr
ENST00000562464.1:n.332-319C>A
ENST00000563655.5:c.241-319C>A	ENSP00000456012.1:n.241-319C>A
ENST00000567391.5:c.188-319C>A	ENSP00000457964.1:n.188-319C>A
ENST00000567713.5:c.277C>A	ENSP00000455749.1:p.Pro93Thr
ENST00000568319.5:c.188-319C>A	ENSP00000456905.1:n.188-319C>A
ENST00000569616.1:c.275C>A
NM_000485.2:c.277C>A	NP_000476.1:p.Pro93Thr
NM_001030018.1:c.277C>A	NP_001025189.1:p.Pro93Thr
NM_000485.3:c.277C>A MANE Select	NP_000476.1:p.Pro93Thr
NM_001030018.2:c.277C>A	NP_001025189.1:p.Pro93Thr