Canonical Allele Identifier: CA485450074
Gene: APEX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.20925265G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20457106G>A , CM000676.2:g.20457106G>A GRCh38
NC_000014.8:g.20925265G>A , CM000676.1:g.20925265G>A GRCh37
NC_000014.7:g.19995105G>A NCBI36
NG_008718.1:g.6976G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216714.8:c.555G>A MANE Select ENSP00000216714.3:p.Arg185=
ENST00000216714.7:c.555G>A ENSP00000216714.3:p.Arg185=
ENST00000398030.8:c.555G>A ENSP00000381111.4:p.Arg185=
ENST00000438886.1:c.335G>A
ENST00000553555.5:n.975G>A
ENST00000553681.5:c.555G>A ENSP00000451327.1:p.Arg185=
ENST00000554813.5:n.621G>A
ENST00000555414.5:c.555G>A ENSP00000451979.1:p.Arg185=
ENST00000555839.5:c.468G>A ENSP00000452460.1:p.Arg156=
ENST00000557054.1:c.28-17G>A ENSP00000452212.2:n.28-17G>A
ENST00000557159.5:n.1171G>A
ENST00000557365.1:n.635G>A
ENST00000557592.5:c.504G>A ENSP00000451060.1:p.Arg168=
NM_001244249.1:c.555G>A NP_001231178.1:p.Arg185=
NM_001641.3:c.555G>A NP_001632.2:p.Arg185=
NM_080648.2:c.555G>A NP_542379.1:p.Arg185=
NM_080649.2:c.555G>A NP_542380.1:p.Arg185=
XM_005267581.3:c.555G>A XP_005267638.1:p.Arg185=
XM_005267582.3:c.504G>A XP_005267639.1:p.Arg168=
NM_001641.4:c.555G>A MANE Select NP_001632.2:p.Arg185=
NM_001244249.2:c.555G>A NP_001231178.1:p.Arg185=
NM_080648.3:c.555G>A NP_542379.1:p.Arg185=
NM_080649.3:c.555G>A NP_542380.1:p.Arg185=