Canonical Allele Identifier: CA2122042090
Gene: APEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20457271C= , CM000676.2:g.20457271C= GRCh38
NC_000014.8:g.20925430C= , CM000676.1:g.20925430C= GRCh37
NC_000014.7:g.19995270C= NCBI36
NG_008718.1:g.7141C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216714.8:c.720C= MANE Select ENSP00000216714.3:p.Phe240=
ENST00000216714.7:c.720C= ENSP00000216714.3:p.Phe240=
ENST00000398030.8:c.720C= ENSP00000381111.4:p.Phe240=
ENST00000553555.5:n.1140C=
ENST00000553681.5:c.720C= ENSP00000451327.1:p.Phe240=
ENST00000555414.5:c.720C= ENSP00000451979.1:p.Phe240=
ENST00000555839.5:c.633C= ENSP00000452460.1:p.Phe211=
ENST00000557054.1:c.*131C= ENSP00000452212.2:n.*131C=
ENST00000557159.5:n.1336C=
ENST00000557365.1:n.800C=
NM_001244249.1:c.720C= NP_001231178.1:p.Phe240=
NM_001641.3:c.720C= NP_001632.2:p.Phe240=
NM_080648.2:c.720C= NP_542379.1:p.Phe240=
NM_080649.2:c.720C= NP_542380.1:p.Phe240=
XM_005267581.3:c.720C= XP_005267638.1:p.Phe240=
XM_005267582.3:c.669C= XP_005267639.1:p.Phe223=
NM_001641.4:c.720C= MANE Select NP_001632.2:p.Phe240=
NM_001244249.2:c.720C= NP_001231178.1:p.Phe240=
NM_080648.3:c.720C= NP_542379.1:p.Phe240=
NM_080649.3:c.720C= NP_542380.1:p.Phe240=