Canonical Allele Identifier: CA389132655
Gene: APEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20457195A>T , CM000676.2:g.20457195A>T GRCh38
NC_000014.8:g.20925354A>T , CM000676.1:g.20925354A>T GRCh37
NC_000014.7:g.19995194A>T NCBI36
NG_008718.1:g.7065A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000216714.8:c.644A>T MANE Select ENSP00000216714.3:p.His215Leu
ENST00000216714.7:c.644A>T ENSP00000216714.3:p.His215Leu
ENST00000398030.8:c.644A>T ENSP00000381111.4:p.His215Leu
ENST00000438886.1:c.424A>T
ENST00000553555.5:n.1064A>T
ENST00000553681.5:c.644A>T ENSP00000451327.1:p.His215Leu
ENST00000555414.5:c.644A>T ENSP00000451979.1:p.His215Leu
ENST00000555839.5:c.557A>T ENSP00000452460.1:p.His186Leu
ENST00000557054.1:c.*55A>T ENSP00000452212.2:n.*55A>T
ENST00000557159.5:n.1260A>T
ENST00000557365.1:n.724A>T
NM_001244249.1:c.644A>T NP_001231178.1:p.His215Leu
NM_001641.3:c.644A>T NP_001632.2:p.His215Leu
NM_080648.2:c.644A>T NP_542379.1:p.His215Leu
NM_080649.2:c.644A>T NP_542380.1:p.His215Leu
XM_005267581.3:c.644A>T XP_005267638.1:p.His215Leu
XM_005267582.3:c.593A>T XP_005267639.1:p.His198Leu
NM_001641.4:c.644A>T MANE Select NP_001632.2:p.His215Leu
NM_001244249.2:c.644A>T NP_001231178.1:p.His215Leu
NM_080648.3:c.644A>T NP_542379.1:p.His215Leu
NM_080649.3:c.644A>T NP_542380.1:p.His215Leu