Canonical Allele Identifier: CA389132738
Gene: APEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20457209C>A , CM000676.2:g.20457209C>A GRCh38
NC_000014.8:g.20925368C>A , CM000676.1:g.20925368C>A GRCh37
NC_000014.7:g.19995208C>A NCBI36
NG_008718.1:g.7079C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216714.8:c.658C>A MANE Select ENSP00000216714.3:p.Leu220Ile
ENST00000216714.7:c.658C>A ENSP00000216714.3:p.Leu220Ile
ENST00000398030.8:c.658C>A ENSP00000381111.4:p.Leu220Ile
ENST00000438886.1:c.438C>A
ENST00000553555.5:n.1078C>A
ENST00000553681.5:c.658C>A ENSP00000451327.1:p.Leu220Ile
ENST00000555414.5:c.658C>A ENSP00000451979.1:p.Leu220Ile
ENST00000555839.5:c.571C>A ENSP00000452460.1:p.Leu191Ile
ENST00000557054.1:c.*69C>A ENSP00000452212.2:n.*69C>A
ENST00000557159.5:n.1274C>A
ENST00000557365.1:n.738C>A
NM_001244249.1:c.658C>A NP_001231178.1:p.Leu220Ile
NM_001641.3:c.658C>A NP_001632.2:p.Leu220Ile
NM_080648.2:c.658C>A NP_542379.1:p.Leu220Ile
NM_080649.2:c.658C>A NP_542380.1:p.Leu220Ile
XM_005267581.3:c.658C>A XP_005267638.1:p.Leu220Ile
XM_005267582.3:c.607C>A XP_005267639.1:p.Leu203Ile
NM_001641.4:c.658C>A MANE Select NP_001632.2:p.Leu220Ile
NM_001244249.2:c.658C>A NP_001231178.1:p.Leu220Ile
NM_080648.3:c.658C>A NP_542379.1:p.Leu220Ile
NM_080649.3:c.658C>A NP_542380.1:p.Leu220Ile