Canonical Allele Identifier: CA2122039914
Gene: APEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20456080G= , CM000676.2:g.20456080G= GRCh38
NC_000014.8:g.20924239G= , CM000676.1:g.20924239G= GRCh37
NC_000014.7:g.19994079G= NCBI36
NG_008718.1:g.5950G=

Transcript Alleles

HGVS Amino-acid change
ENST00000216714.8:c.225G= MANE Select ENSP00000216714.3:p.Trp75=
ENST00000216714.7:c.225G= ENSP00000216714.3:p.Trp75=
ENST00000398030.8:c.225G= ENSP00000381111.4:p.Trp75=
ENST00000438886.1:c.74G=
ENST00000553555.5:n.645G=
ENST00000553681.5:c.225G= ENSP00000451327.1:p.Trp75=
ENST00000554325.1:c.*145G= ENSP00000450604.1:n.*145G=
ENST00000554813.5:n.291G=
ENST00000555306.5:n.672G=
ENST00000555414.5:c.225G= ENSP00000451979.1:p.Trp75=
ENST00000555839.5:c.225G= ENSP00000452460.1:p.Trp75=
ENST00000556054.5:c.225G= ENSP00000451170.1:p.Trp75=
ENST00000557054.1:c.27+408G= ENSP00000452212.2:n.27+408G=
ENST00000557150.5:c.174G= ENSP00000452418.1:p.Trp58=
ENST00000557159.5:n.841G=
ENST00000557181.5:c.225G= ENSP00000452304.1:p.Trp75=
ENST00000557344.5:c.225G= ENSP00000452137.1:p.Trp75=
ENST00000557365.1:n.305G=
ENST00000557592.5:c.174G= ENSP00000451060.1:p.Trp58=
NM_001244249.1:c.225G= NP_001231178.1:p.Trp75=
NM_001641.3:c.225G= NP_001632.2:p.Trp75=
NM_080648.2:c.225G= NP_542379.1:p.Trp75=
NM_080649.2:c.225G= NP_542380.1:p.Trp75=
XM_005267581.3:c.225G= XP_005267638.1:p.Trp75=
XM_005267582.3:c.174G= XP_005267639.1:p.Trp58=
NM_001641.4:c.225G= MANE Select NP_001632.2:p.Trp75=
NM_001244249.2:c.225G= NP_001231178.1:p.Trp75=
NM_080648.3:c.225G= NP_542379.1:p.Trp75=
NM_080649.3:c.225G= NP_542380.1:p.Trp75=