Canonical Allele Identifier: CA645584522

Gene: APRT

Linked Data

• COSMIC: COSM5505009 ; COSM5505010 ; COSM5505011

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810458_88810459insCC , CM000678.2:g.88810458_88810459insCC	GRCh38
NC_000016.9:g.88876866_88876867insCC , CM000678.1:g.88876866_88876867insCC	GRCh37
NC_000016.8:g.87404367_87404368insCC	NCBI36
NG_008013.1:g.6476_6477insGG
NG_028266.1:g.11681_11682insCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000378364.8:c.285_286insGG MANE Select	ENSP00000367615.3:p.Thr96GlyfsTer?
ENST00000378364.7:c.285_286insGG	ENSP00000367615.3:p.Thr96GlyfsTer?
ENST00000426324.6:c.285_286insGG	ENSP00000397007.2:p.Thr96GlyfsTer?
ENST00000562464.1:n.332-311_332-310insGG
ENST00000563655.5:c.241-311_241-310insGG	ENSP00000456012.1:n.241-311_241-310insGG
ENST00000567391.5:c.188-311_188-310insGG	ENSP00000457964.1:n.188-311_188-310insGG
ENST00000567713.5:c.285_286insGG	ENSP00000455749.1:p.Thr96GlyfsTer30
ENST00000568319.5:c.188-311_188-310insGG	ENSP00000456905.1:n.188-311_188-310insGG
ENST00000569616.1:c.283_284insGG
NM_000485.2:c.285_286insGG	NP_000476.1:p.Thr96GlyfsTer?
NM_001030018.1:c.285_286insGG	NP_001025189.1:p.Thr96GlyfsTer?
NM_000485.3:c.285_286insGG MANE Select	NP_000476.1:p.Thr96GlyfsTer?
NM_001030018.2:c.285_286insGG	NP_001025189.1:p.Thr96GlyfsTer?