Canonical Allele Identifier: CA389130784
Gene: APEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20456764T>G , CM000676.2:g.20456764T>G GRCh38
NC_000014.8:g.20924923T>G , CM000676.1:g.20924923T>G GRCh37
NC_000014.7:g.19994763T>G NCBI36
NG_008718.1:g.6634T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216714.8:c.343T>G MANE Select ENSP00000216714.3:p.Ser115Ala
ENST00000216714.7:c.343T>G ENSP00000216714.3:p.Ser115Ala
ENST00000398030.8:c.343T>G ENSP00000381111.4:p.Ser115Ala
ENST00000438886.1:c.192T>G
ENST00000553555.5:n.763T>G
ENST00000553681.5:c.343T>G ENSP00000451327.1:p.Ser115Ala
ENST00000554813.5:n.409T>G
ENST00000555306.5:n.790T>G
ENST00000555414.5:c.343T>G ENSP00000451979.1:p.Ser115Ala
ENST00000555839.5:c.343T>G ENSP00000452460.1:p.Ser115Ala
ENST00000556054.5:c.343T>G ENSP00000451170.1:p.Ser115Ala
ENST00000557054.1:c.28-359T>G ENSP00000452212.2:n.28-359T>G
ENST00000557150.5:c.292T>G ENSP00000452418.1:p.Ser98Ala
ENST00000557159.5:n.959T>G
ENST00000557344.5:c.343T>G ENSP00000452137.1:p.Ser115Ala
ENST00000557365.1:n.423T>G
ENST00000557592.5:c.292T>G ENSP00000451060.1:p.Ser98Ala
NM_001244249.1:c.343T>G NP_001231178.1:p.Ser115Ala
NM_001641.3:c.343T>G NP_001632.2:p.Ser115Ala
NM_080648.2:c.343T>G NP_542379.1:p.Ser115Ala
NM_080649.2:c.343T>G NP_542380.1:p.Ser115Ala
XM_005267581.3:c.343T>G XP_005267638.1:p.Ser115Ala
XM_005267582.3:c.292T>G XP_005267639.1:p.Ser98Ala
NM_001641.4:c.343T>G MANE Select NP_001632.2:p.Ser115Ala
NM_001244249.2:c.343T>G NP_001231178.1:p.Ser115Ala
NM_080648.3:c.343T>G NP_542379.1:p.Ser115Ala
NM_080649.3:c.343T>G NP_542380.1:p.Ser115Ala