Canonical Allele Identifier: CA389132166
Gene: APEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20457121A>G , CM000676.2:g.20457121A>G GRCh38
NC_000014.8:g.20925280A>G , CM000676.1:g.20925280A>G GRCh37
NC_000014.7:g.19995120A>G NCBI36
NG_008718.1:g.6991A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216714.8:c.570A>G MANE Select ENSP00000216714.3:p.Glu190=
ENST00000216714.7:c.570A>G ENSP00000216714.3:p.Glu190=
ENST00000398030.8:c.570A>G ENSP00000381111.4:p.Glu190=
ENST00000438886.1:c.350A>G
ENST00000553555.5:n.990A>G
ENST00000553681.5:c.570A>G ENSP00000451327.1:p.Glu190=
ENST00000554813.5:n.636A>G
ENST00000555414.5:c.570A>G ENSP00000451979.1:p.Glu190=
ENST00000555839.5:c.483A>G ENSP00000452460.1:p.Glu161=
ENST00000557054.1:c.28-2A>G ENSP00000452212.2:n.28-2A>G
ENST00000557159.5:n.1186A>G
ENST00000557365.1:n.650A>G
NM_001244249.1:c.570A>G NP_001231178.1:p.Glu190=
NM_001641.3:c.570A>G NP_001632.2:p.Glu190=
NM_080648.2:c.570A>G NP_542379.1:p.Glu190=
NM_080649.2:c.570A>G NP_542380.1:p.Glu190=
XM_005267581.3:c.570A>G XP_005267638.1:p.Glu190=
XM_005267582.3:c.519A>G XP_005267639.1:p.Glu173=
NM_001641.4:c.570A>G MANE Select NP_001632.2:p.Glu190=
NM_001244249.2:c.570A>G NP_001231178.1:p.Glu190=
NM_080648.3:c.570A>G NP_542379.1:p.Glu190=
NM_080649.3:c.570A>G NP_542380.1:p.Glu190=