Canonical Allele Identifier: CA389132274
Gene: APEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20457139G>C , CM000676.2:g.20457139G>C GRCh38
NC_000014.8:g.20925298G>C , CM000676.1:g.20925298G>C GRCh37
NC_000014.7:g.19995138G>C NCBI36
NG_008718.1:g.7009G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216714.8:c.588G>C MANE Select ENSP00000216714.3:p.Leu196=
ENST00000216714.7:c.588G>C ENSP00000216714.3:p.Leu196=
ENST00000398030.8:c.588G>C ENSP00000381111.4:p.Leu196=
ENST00000438886.1:c.368G>C
ENST00000553555.5:n.1008G>C
ENST00000553681.5:c.588G>C ENSP00000451327.1:p.Leu196=
ENST00000554813.5:n.654G>C
ENST00000555414.5:c.588G>C ENSP00000451979.1:p.Leu196=
ENST00000555839.5:c.501G>C ENSP00000452460.1:p.Leu167=
ENST00000557054.1:c.44G>C ENSP00000452212.2:p.Ter15Ser
ENST00000557159.5:n.1204G>C
ENST00000557365.1:n.668G>C
NM_001244249.1:c.588G>C NP_001231178.1:p.Leu196=
NM_001641.3:c.588G>C NP_001632.2:p.Leu196=
NM_080648.2:c.588G>C NP_542379.1:p.Leu196=
NM_080649.2:c.588G>C NP_542380.1:p.Leu196=
XM_005267581.3:c.588G>C XP_005267638.1:p.Leu196=
XM_005267582.3:c.537G>C XP_005267639.1:p.Leu179=
NM_001641.4:c.588G>C MANE Select NP_001632.2:p.Leu196=
NM_001244249.2:c.588G>C NP_001231178.1:p.Leu196=
NM_080648.3:c.588G>C NP_542379.1:p.Leu196=
NM_080649.3:c.588G>C NP_542380.1:p.Leu196=