Canonical Allele Identifier: CA397087829

Gene: APRT

Linked Data

• gnomAD v4: 16-88810103-C-T
• MyVariant Identifiers: chr16:g.88876511C>T (hg19) ; chr16:g.88810103C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810103C>T , CM000678.2:g.88810103C>T	GRCh38
NC_000016.9:g.88876511C>T , CM000678.1:g.88876511C>T	GRCh37
NC_000016.8:g.87404012C>T	NCBI36
NG_008013.1:g.6832G>A
NG_028266.1:g.11326C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.367G>A MANE Select	ENSP00000367615.3:p.Val123Met
ENST00000378364.7:c.367G>A	ENSP00000367615.3:p.Val123Met
ENST00000426324.6:c.367G>A	ENSP00000397007.2:p.Val123Met
ENST00000562464.1:n.377G>A
ENST00000563655.5:c.286G>A	ENSP00000456012.1:p.Val96Met
ENST00000567057.5:n.166G>A
ENST00000567391.5:c.*41G>A	ENSP00000457964.1:n.*41G>A
ENST00000567713.5:c.321+320G>A	ENSP00000455749.1:n.321+320G>A
ENST00000568319.5:c.*41G>A	ENSP00000456905.1:n.*41G>A
ENST00000568575.1:n.296G>A
ENST00000569616.1:c.365G>A
NM_000485.2:c.367G>A	NP_000476.1:p.Val123Met
NM_001030018.1:c.367G>A	NP_001025189.1:p.Val123Met
NM_000485.3:c.367G>A MANE Select	NP_000476.1:p.Val123Met
NM_001030018.2:c.367G>A	NP_001025189.1:p.Val123Met