Canonical Allele Identifier: CA497086255

Gene: APRT

Linked Data

• MyVariant Identifiers: chr16:g.88876542A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810134A>G , CM000678.2:g.88810134A>G	GRCh38
NC_000016.9:g.88876542A>G , CM000678.1:g.88876542A>G	GRCh37
NC_000016.8:g.87404043A>G	NCBI36
NG_008013.1:g.6801T>C
NG_028266.1:g.11357A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.336T>C MANE Select	ENSP00000367615.3:p.Ile112=
ENST00000378364.7:c.336T>C	ENSP00000367615.3:p.Ile112=
ENST00000426324.6:c.336T>C	ENSP00000397007.2:p.Ile112=
ENST00000562464.1:n.346T>C
ENST00000563655.5:c.255T>C	ENSP00000456012.1:p.Ile85=
ENST00000567057.5:n.135T>C
ENST00000567391.5:c.*10T>C	ENSP00000457964.1:n.*10T>C
ENST00000567713.5:c.321+289T>C	ENSP00000455749.1:n.321+289T>C
ENST00000568319.5:c.*10T>C	ENSP00000456905.1:n.*10T>C
ENST00000568575.1:n.265T>C
ENST00000569616.1:c.334T>C
NM_000485.2:c.336T>C	NP_000476.1:p.Ile112=
NM_001030018.1:c.336T>C	NP_001025189.1:p.Ile112=
NM_000485.3:c.336T>C MANE Select	NP_000476.1:p.Ile112=
NM_001030018.2:c.336T>C	NP_001025189.1:p.Ile112=