Canonical Allele Identifier: CA397086084

Gene: APRT

Linked Data

• MyVariant Identifiers: chr16:g.88876114A>G (hg19) ; chr16:g.88809706A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809706A>G , CM000678.2:g.88809706A>G	GRCh38
NC_000016.9:g.88876114A>G , CM000678.1:g.88876114A>G	GRCh37
NC_000016.8:g.87403615A>G	NCBI36
NG_008013.1:g.7229T>C
NG_028266.1:g.10929A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.535T>C MANE Select	ENSP00000367615.3:p.Tyr179His
ENST00000378364.7:c.535T>C	ENSP00000367615.3:p.Tyr179His
ENST00000426324.6:c.401T>C	ENSP00000397007.2:p.Val134Ala
ENST00000563655.5:c.454T>C	ENSP00000456012.1:p.Tyr152His
ENST00000567057.5:n.200T>C
ENST00000567391.5:c.*209T>C	ENSP00000457964.1:n.*209T>C
ENST00000567713.5:c.322-171T>C	ENSP00000455749.1:n.322-171T>C
ENST00000568319.5:c.*75T>C	ENSP00000456905.1:n.*75T>C
ENST00000568575.1:n.464T>C
ENST00000569616.1:c.600T>C
NM_000485.2:c.535T>C	NP_000476.1:p.Tyr179His
NM_001030018.1:c.401T>C	NP_001025189.1:p.Val134Ala
NM_000485.3:c.535T>C MANE Select	NP_000476.1:p.Tyr179His
NM_001030018.2:c.401T>C	NP_001025189.1:p.Val134Ala