Canonical Allele Identifier: CA2122040872
Gene: APEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20456700C= , CM000676.2:g.20456700C= GRCh38
NC_000014.8:g.20924859C= , CM000676.1:g.20924859C= GRCh37
NC_000014.7:g.19994699C= NCBI36
NG_008718.1:g.6570C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216714.8:c.279C= MANE Select ENSP00000216714.3:p.Cys93=
ENST00000216714.7:c.279C= ENSP00000216714.3:p.Cys93=
ENST00000398030.8:c.279C= ENSP00000381111.4:p.Cys93=
ENST00000438886.1:c.128C=
ENST00000553555.5:n.699C=
ENST00000553681.5:c.279C= ENSP00000451327.1:p.Cys93=
ENST00000554813.5:n.345C=
ENST00000555306.5:n.726C=
ENST00000555414.5:c.279C= ENSP00000451979.1:p.Cys93=
ENST00000555839.5:c.279C= ENSP00000452460.1:p.Cys93=
ENST00000556054.5:c.279C= ENSP00000451170.1:p.Cys93=
ENST00000557054.1:c.28-423C= ENSP00000452212.2:n.28-423C=
ENST00000557150.5:c.228C= ENSP00000452418.1:p.Cys76=
ENST00000557159.5:n.895C=
ENST00000557181.5:c.279C= ENSP00000452304.1:p.Cys93=
ENST00000557344.5:c.279C= ENSP00000452137.1:p.Cys93=
ENST00000557365.1:n.359C=
ENST00000557592.5:c.228C= ENSP00000451060.1:p.Cys76=
NM_001244249.1:c.279C= NP_001231178.1:p.Cys93=
NM_001641.3:c.279C= NP_001632.2:p.Cys93=
NM_080648.2:c.279C= NP_542379.1:p.Cys93=
NM_080649.2:c.279C= NP_542380.1:p.Cys93=
XM_005267581.3:c.279C= XP_005267638.1:p.Cys93=
XM_005267582.3:c.228C= XP_005267639.1:p.Cys76=
NM_001641.4:c.279C= MANE Select NP_001632.2:p.Cys93=
NM_001244249.2:c.279C= NP_001231178.1:p.Cys93=
NM_080648.3:c.279C= NP_542379.1:p.Cys93=
NM_080649.3:c.279C= NP_542380.1:p.Cys93=