Canonical Allele Identifier: CA8234337

Gene: APRT

Linked Data

• dbSNP Id: rs375180338
• ExAC: 16:88876104 G / A
• gnomAD v2: 16-88876104-G-A
• gnomAD v3: 16-88809696-G-A
• gnomAD v4: 16-88809696-G-A
• MyVariant Identifiers: chr16:g.88876104G>A (hg19) ; chr16:g.88809696G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809696G>A , CM000678.2:g.88809696G>A	GRCh38
NC_000016.9:g.88876104G>A , CM000678.1:g.88876104G>A	GRCh37
NC_000016.8:g.87403605G>A	NCBI36
NG_008013.1:g.7239C>T
NG_028266.1:g.10919G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.*2C>T MANE Select	ENSP00000367615.3:n.*2C>T
ENST00000378364.7:c.*2C>T	ENSP00000367615.3:n.*2C>T
ENST00000426324.6:c.*6C>T	ENSP00000397007.2:n.*6C>T
ENST00000563655.5:c.*2C>T	ENSP00000456012.1:n.*2C>T
ENST00000567057.5:n.210C>T
ENST00000567391.5:c.*219C>T	ENSP00000457964.1:n.*219C>T
ENST00000567713.5:c.322-161C>T	ENSP00000455749.1:n.322-161C>T
ENST00000568319.5:c.*85C>T	ENSP00000456905.1:n.*85C>T
ENST00000568575.1:n.474C>T
ENST00000569616.1:c.610C>T
NM_000485.2:c.*2C>T	NP_000476.1:n.*2C>T
NM_001030018.1:c.*6C>T	NP_001025189.1:n.*6C>T
NM_000485.3:c.*2C>T MANE Select	NP_000476.1:n.*2C>T
NM_001030018.2:c.*6C>T	NP_001025189.1:n.*6C>T