Canonical Allele Identifier: CA2122041800
Gene: APEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20457133G= , CM000676.2:g.20457133G= GRCh38
NC_000014.8:g.20925292G= , CM000676.1:g.20925292G= GRCh37
NC_000014.7:g.19995132G= NCBI36
NG_008718.1:g.7003G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216714.8:c.582G= MANE Select ENSP00000216714.3:p.Lys194=
ENST00000216714.7:c.582G= ENSP00000216714.3:p.Lys194=
ENST00000398030.8:c.582G= ENSP00000381111.4:p.Lys194=
ENST00000438886.1:c.362G=
ENST00000553555.5:n.1002G=
ENST00000553681.5:c.582G= ENSP00000451327.1:p.Lys194=
ENST00000554813.5:n.648G=
ENST00000555414.5:c.582G= ENSP00000451979.1:p.Lys194=
ENST00000555839.5:c.495G= ENSP00000452460.1:p.Lys165=
ENST00000557054.1:c.38G= ENSP00000452212.2:p.Ser13=
ENST00000557159.5:n.1198G=
ENST00000557365.1:n.662G=
NM_001244249.1:c.582G= NP_001231178.1:p.Lys194=
NM_001641.3:c.582G= NP_001632.2:p.Lys194=
NM_080648.2:c.582G= NP_542379.1:p.Lys194=
NM_080649.2:c.582G= NP_542380.1:p.Lys194=
XM_005267581.3:c.582G= XP_005267638.1:p.Lys194=
XM_005267582.3:c.531G= XP_005267639.1:p.Lys177=
NM_001641.4:c.582G= MANE Select NP_001632.2:p.Lys194=
NM_001244249.2:c.582G= NP_001231178.1:p.Lys194=
NM_080648.3:c.582G= NP_542379.1:p.Lys194=
NM_080649.3:c.582G= NP_542380.1:p.Lys194=