Canonical Allele Identifier: CA8234334

Gene: APRT

Linked Data

• dbSNP Id: rs374275550
• ExAC: 16:88876092 G / A
• gnomAD v2: 16-88876092-G-A
• gnomAD v3: 16-88809684-G-A
• gnomAD v4: 16-88809684-G-A
• MyVariant Identifiers: chr16:g.88876092G>A (hg19) ; chr16:g.88809684G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809684G>A , CM000678.2:g.88809684G>A	GRCh38
NC_000016.9:g.88876092G>A , CM000678.1:g.88876092G>A	GRCh37
NC_000016.8:g.87403593G>A	NCBI36
NG_008013.1:g.7251C>T
NG_028266.1:g.10907G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.*14C>T MANE Select	ENSP00000367615.3:n.*14C>T
ENST00000378364.7:c.*14C>T	ENSP00000367615.3:n.*14C>T
ENST00000426324.6:c.*18C>T	ENSP00000397007.2:n.*18C>T
ENST00000563655.5:c.*14C>T	ENSP00000456012.1:n.*14C>T
ENST00000567057.5:n.222C>T
ENST00000567391.5:c.*231C>T	ENSP00000457964.1:n.*231C>T
ENST00000567713.5:c.322-149C>T	ENSP00000455749.1:n.322-149C>T
ENST00000568319.5:c.*97C>T	ENSP00000456905.1:n.*97C>T
ENST00000568575.1:n.486C>T
ENST00000569616.1:c.622C>T
NM_000485.2:c.*14C>T	NP_000476.1:n.*14C>T
NM_001030018.1:c.*18C>T	NP_001025189.1:n.*18C>T
NM_000485.3:c.*14C>T MANE Select	NP_000476.1:n.*14C>T
NM_001030018.2:c.*18C>T	NP_001025189.1:n.*18C>T