Canonical Allele Identifier: CA389131975
Gene: APEX1 HGNC NCBI

Linked Data

dbSNP Id: rs1239749291

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20457080C>T , CM000676.2:g.20457080C>T GRCh38
NC_000014.8:g.20925239C>T , CM000676.1:g.20925239C>T GRCh37
NC_000014.7:g.19995079C>T NCBI36
NG_008718.1:g.6950C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000216714.8:c.529C>T MANE Select ENSP00000216714.3:p.Arg177Ter
ENST00000216714.7:c.529C>T ENSP00000216714.3:p.Arg177Ter
ENST00000398030.8:c.529C>T ENSP00000381111.4:p.Arg177Ter
ENST00000438886.1:c.309C>T
ENST00000553555.5:n.949C>T
ENST00000553681.5:c.529C>T ENSP00000451327.1:p.Arg177Ter
ENST00000554813.5:n.595C>T
ENST00000555414.5:c.529C>T ENSP00000451979.1:p.Arg177Ter
ENST00000555839.5:c.442C>T ENSP00000452460.1:p.Arg148Ter
ENST00000557054.1:c.28-43C>T ENSP00000452212.2:n.28-43C>T
ENST00000557150.5:c.478C>T ENSP00000452418.1:p.Arg160Ter
ENST00000557159.5:n.1145C>T
ENST00000557365.1:n.609C>T
ENST00000557592.5:c.478C>T ENSP00000451060.1:p.Arg160Ter
NM_001244249.1:c.529C>T NP_001231178.1:p.Arg177Ter
NM_001641.3:c.529C>T NP_001632.2:p.Arg177Ter
NM_080648.2:c.529C>T NP_542379.1:p.Arg177Ter
NM_080649.2:c.529C>T NP_542380.1:p.Arg177Ter
XM_005267581.3:c.529C>T XP_005267638.1:p.Arg177Ter
XM_005267582.3:c.478C>T XP_005267639.1:p.Arg160Ter
NM_001641.4:c.529C>T MANE Select NP_001632.2:p.Arg177Ter
NM_001244249.2:c.529C>T NP_001231178.1:p.Arg177Ter
NM_080648.3:c.529C>T NP_542379.1:p.Arg177Ter
NM_080649.3:c.529C>T NP_542380.1:p.Arg177Ter