Canonical Allele Identifier: CA389131064
Gene: APEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20456835C>A , CM000676.2:g.20456835C>A GRCh38
NC_000014.8:g.20924994C>A , CM000676.1:g.20924994C>A GRCh37
NC_000014.7:g.19994834C>A NCBI36
NG_008718.1:g.6705C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216714.8:c.414C>A MANE Select ENSP00000216714.3:p.Cys138Ter
ENST00000216714.7:c.414C>A ENSP00000216714.3:p.Cys138Ter
ENST00000398030.8:c.414C>A ENSP00000381111.4:p.Cys138Ter
ENST00000438886.1:c.263C>A
ENST00000553555.5:n.834C>A
ENST00000553681.5:c.414C>A ENSP00000451327.1:p.Cys138Ter
ENST00000554813.5:n.480C>A
ENST00000555306.5:n.861C>A
ENST00000555414.5:c.414C>A ENSP00000451979.1:p.Cys138Ter
ENST00000555839.5:c.414C>A ENSP00000452460.1:p.Cys138Ter
ENST00000556054.5:c.414C>A ENSP00000451170.1:p.Cys138Ter
ENST00000557054.1:c.28-288C>A ENSP00000452212.2:n.28-288C>A
ENST00000557150.5:c.363C>A ENSP00000452418.1:p.Cys121Ter
ENST00000557159.5:n.1030C>A
ENST00000557344.5:c.414C>A ENSP00000452137.1:p.Cys138Ter
ENST00000557365.1:n.494C>A
ENST00000557592.5:c.363C>A ENSP00000451060.1:p.Cys121Ter
NM_001244249.1:c.414C>A NP_001231178.1:p.Cys138Ter
NM_001641.3:c.414C>A NP_001632.2:p.Cys138Ter
NM_080648.2:c.414C>A NP_542379.1:p.Cys138Ter
NM_080649.2:c.414C>A NP_542380.1:p.Cys138Ter
XM_005267581.3:c.414C>A XP_005267638.1:p.Cys138Ter
XM_005267582.3:c.363C>A XP_005267639.1:p.Cys121Ter
NM_001641.4:c.414C>A MANE Select NP_001632.2:p.Cys138Ter
NM_001244249.2:c.414C>A NP_001231178.1:p.Cys138Ter
NM_080648.3:c.414C>A NP_542379.1:p.Cys138Ter
NM_080649.3:c.414C>A NP_542380.1:p.Cys138Ter