Canonical Allele Identifier: CA2739267018

Gene: APRT

Linked Data

• ClinVar Variation Id: 2840982
• ClinVar RCV Id: RCV003718786

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810052C>T , CM000678.2:g.88810052C>T	GRCh38
NC_000016.9:g.88876460C>T , CM000678.1:g.88876460C>T	GRCh37
NC_000016.8:g.87403961C>T	NCBI36
NG_008013.1:g.6883G>A
NG_028266.1:g.11275C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.400+18G>A MANE Select	ENSP00000367615.3:n.400+18G>A
ENST00000378364.7:c.400+18G>A	ENSP00000367615.3:n.400+18G>A
ENST00000426324.6:c.400+18G>A	ENSP00000397007.2:n.400+18G>A
ENST00000562464.1:n.410+18G>A
ENST00000563655.5:c.319+18G>A	ENSP00000456012.1:n.319+18G>A
ENST00000567057.5:n.199+18G>A
ENST00000567391.5:c.*74+18G>A	ENSP00000457964.1:n.*74+18G>A
ENST00000567713.5:c.321+371G>A	ENSP00000455749.1:n.321+371G>A
ENST00000568319.5:c.*74+18G>A	ENSP00000456905.1:n.*74+18G>A
ENST00000568575.1:n.329+18G>A
ENST00000569616.1:c.398+18G>A
NM_000485.2:c.400+18G>A	NP_000476.1:n.400+18G>A
NM_001030018.1:c.400+18G>A	NP_001025189.1:n.400+18G>A
NM_000485.3:c.400+18G>A MANE Select	NP_000476.1:n.400+18G>A
NM_001030018.2:c.400+18G>A	NP_001025189.1:n.400+18G>A