Canonical Allele Identifier: CA2634887078

Gene: APRT

Linked Data

• gnomAD v4: 16-88809688-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809688G>A , CM000678.2:g.88809688G>A	GRCh38
NC_000016.9:g.88876096G>A , CM000678.1:g.88876096G>A	GRCh37
NC_000016.8:g.87403597G>A	NCBI36
NG_008013.1:g.7247C>T
NG_028266.1:g.10911G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.*10C>T MANE Select	ENSP00000367615.3:n.*10C>T
ENST00000378364.7:c.*10C>T	ENSP00000367615.3:n.*10C>T
ENST00000426324.6:c.*14C>T	ENSP00000397007.2:n.*14C>T
ENST00000563655.5:c.*10C>T	ENSP00000456012.1:n.*10C>T
ENST00000567057.5:n.218C>T
ENST00000567391.5:c.*227C>T	ENSP00000457964.1:n.*227C>T
ENST00000567713.5:c.322-153C>T	ENSP00000455749.1:n.322-153C>T
ENST00000568319.5:c.*93C>T	ENSP00000456905.1:n.*93C>T
ENST00000568575.1:n.482C>T
ENST00000569616.1:c.618C>T
NM_000485.2:c.*10C>T	NP_000476.1:n.*10C>T
NM_001030018.1:c.*14C>T	NP_001025189.1:n.*14C>T
NM_000485.3:c.*10C>T MANE Select	NP_000476.1:n.*10C>T
NM_001030018.2:c.*14C>T	NP_001025189.1:n.*14C>T