Canonical Allele Identifier: CA397088632

Gene: APRT

Linked Data

• MyVariant Identifiers: chr16:g.88876920C>A (hg19) ; chr16:g.88810512C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810512C>A , CM000678.2:g.88810512C>A	GRCh38
NC_000016.9:g.88876920C>A , CM000678.1:g.88876920C>A	GRCh37
NC_000016.8:g.87404421C>A	NCBI36
NG_008013.1:g.6423G>T
NG_028266.1:g.11735C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.232G>T MANE Select	ENSP00000367615.3:p.Glu78Ter
ENST00000378364.7:c.232G>T	ENSP00000367615.3:p.Glu78Ter
ENST00000426324.6:c.232G>T	ENSP00000397007.2:p.Glu78Ter
ENST00000562464.1:n.332-364G>T
ENST00000563655.5:c.241-364G>T	ENSP00000456012.1:n.241-364G>T
ENST00000567391.5:c.188-364G>T	ENSP00000457964.1:n.188-364G>T
ENST00000567713.5:c.232G>T	ENSP00000455749.1:p.Glu78Ter
ENST00000568319.5:c.188-364G>T	ENSP00000456905.1:n.188-364G>T
ENST00000569616.1:c.230G>T
NM_000485.2:c.232G>T	NP_000476.1:p.Glu78Ter
NM_001030018.1:c.232G>T	NP_001025189.1:p.Glu78Ter
NM_000485.3:c.232G>T MANE Select	NP_000476.1:p.Glu78Ter
NM_001030018.2:c.232G>T	NP_001025189.1:p.Glu78Ter