Canonical Allele Identifier: CA397087606

Gene: APRT

Linked Data

• dbSNP Id: rs1260853080
• gnomAD v2: 16-88876486-G-T
• MyVariant Identifiers: chr16:g.88876486G>T (hg19) ; chr16:g.88810078G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810078G>T , CM000678.2:g.88810078G>T	GRCh38
NC_000016.9:g.88876486G>T , CM000678.1:g.88876486G>T	GRCh37
NC_000016.8:g.87403987G>T	NCBI36
NG_008013.1:g.6857C>A
NG_028266.1:g.11301G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.392C>A MANE Select	ENSP00000367615.3:p.Ala131Asp
ENST00000378364.7:c.392C>A	ENSP00000367615.3:p.Ala131Asp
ENST00000426324.6:c.392C>A	ENSP00000397007.2:p.Ala131Asp
ENST00000562464.1:n.402C>A
ENST00000563655.5:c.311C>A	ENSP00000456012.1:p.Ala104Asp
ENST00000567057.5:n.191C>A
ENST00000567391.5:c.*66C>A	ENSP00000457964.1:n.*66C>A
ENST00000567713.5:c.321+345C>A	ENSP00000455749.1:n.321+345C>A
ENST00000568319.5:c.*66C>A	ENSP00000456905.1:n.*66C>A
ENST00000568575.1:n.321C>A
ENST00000569616.1:c.390C>A
NM_000485.2:c.392C>A	NP_000476.1:p.Ala131Asp
NM_001030018.1:c.392C>A	NP_001025189.1:p.Ala131Asp
NM_000485.3:c.392C>A MANE Select	NP_000476.1:p.Ala131Asp
NM_001030018.2:c.392C>A	NP_001025189.1:p.Ala131Asp