Canonical Allele Identifier: CA980350313

Gene: APRT

Linked Data

• dbSNP Id: rs1909031215
• gnomAD v3: 16-88809685-G-C
• gnomAD v4: 16-88809685-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809685G>C , CM000678.2:g.88809685G>C	GRCh38
NC_000016.9:g.88876093G>C , CM000678.1:g.88876093G>C	GRCh37
NC_000016.8:g.87403594G>C	NCBI36
NG_008013.1:g.7250C>G
NG_028266.1:g.10908G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.*13C>G MANE Select	ENSP00000367615.3:n.*13C>G
ENST00000378364.7:c.*13C>G	ENSP00000367615.3:n.*13C>G
ENST00000426324.6:c.*17C>G	ENSP00000397007.2:n.*17C>G
ENST00000563655.5:c.*13C>G	ENSP00000456012.1:n.*13C>G
ENST00000567057.5:n.221C>G
ENST00000567391.5:c.*230C>G	ENSP00000457964.1:n.*230C>G
ENST00000567713.5:c.322-150C>G	ENSP00000455749.1:n.322-150C>G
ENST00000568319.5:c.*96C>G	ENSP00000456905.1:n.*96C>G
ENST00000568575.1:n.485C>G
ENST00000569616.1:c.621C>G
NM_000485.2:c.*13C>G	NP_000476.1:n.*13C>G
NM_001030018.1:c.*17C>G	NP_001025189.1:n.*17C>G
NM_000485.3:c.*13C>G MANE Select	NP_000476.1:n.*13C>G
NM_001030018.2:c.*17C>G	NP_001025189.1:n.*17C>G