Canonical Allele Identifier: CA257407659
Gene: APEX1 HGNC NCBI

Linked Data

dbSNP Id: rs767995071

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20456952_20456955del , CM000676.2:g.20456952_20456955del GRCh38
NC_000014.8:g.20925111_20925114del , CM000676.1:g.20925111_20925114del GRCh37
NC_000014.7:g.19994951_19994954del NCBI36
NG_008718.1:g.6822_6825del

Transcript Alleles

HGVS Amino-acid Change
ENST00000216714.8:c.440-39_440-36del MANE Select ENSP00000216714.3:n.440-39_440-36del
ENST00000216714.7:c.440-39_440-36del ENSP00000216714.3:n.440-39_440-36del
ENST00000398030.8:c.440-39_440-36del ENSP00000381111.4:n.440-39_440-36del
ENST00000438886.1:c.288+92_288+95del
ENST00000553555.5:n.860-39_860-36del
ENST00000553681.5:c.440-39_440-36del ENSP00000451327.1:n.440-39_440-36del
ENST00000554813.5:n.506-39_506-36del
ENST00000555306.5:n.887-39_887-36del
ENST00000555414.5:c.440-39_440-36del ENSP00000451979.1:n.440-39_440-36del
ENST00000555839.5:c.439+92_439+95del ENSP00000452460.1:n.439+92_439+95del
ENST00000556054.5:c.440-39_440-36del ENSP00000451170.1:n.440-39_440-36del
ENST00000557054.1:c.28-171_28-168del ENSP00000452212.2:n.28-171_28-168del
ENST00000557150.5:c.389-39_389-36del ENSP00000452418.1:n.389-39_389-36del
ENST00000557159.5:n.1056-39_1056-36del
ENST00000557365.1:n.520-39_520-36del
ENST00000557592.5:c.389-39_389-36del ENSP00000451060.1:n.389-39_389-36del
NM_001244249.1:c.440-39_440-36del NP_001231178.1:n.440-39_440-36del
NM_001641.3:c.440-39_440-36del NP_001632.2:n.440-39_440-36del
NM_080648.2:c.440-39_440-36del NP_542379.1:n.440-39_440-36del
NM_080649.2:c.440-39_440-36del NP_542380.1:n.440-39_440-36del
XM_005267581.3:c.440-39_440-36del XP_005267638.1:n.440-39_440-36del
XM_005267582.3:c.389-39_389-36del XP_005267639.1:n.389-39_389-36del
NM_001641.4:c.440-39_440-36del MANE Select NP_001632.2:n.440-39_440-36del
NM_001244249.2:c.440-39_440-36del NP_001231178.1:n.440-39_440-36del
NM_080648.3:c.440-39_440-36del NP_542379.1:n.440-39_440-36del
NM_080649.3:c.440-39_440-36del NP_542380.1:n.440-39_440-36del