Canonical Allele Identifier: CA389132054

Gene: APEX1

Linked Data

• MyVariant Identifiers: chr14:g.20925259G>T (hg19) ; chr14:g.20457100G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20457100G>T , CM000676.2:g.20457100G>T	GRCh38
NC_000014.8:g.20925259G>T , CM000676.1:g.20925259G>T	GRCh37
NC_000014.7:g.19995099G>T	NCBI36
NG_008718.1:g.6970G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216714.8:c.549G>T MANE Select	ENSP00000216714.3:p.Glu183Asp
ENST00000216714.7:c.549G>T	ENSP00000216714.3:p.Glu183Asp
ENST00000398030.8:c.549G>T	ENSP00000381111.4:p.Glu183Asp
ENST00000438886.1:c.329G>T
ENST00000553555.5:n.969G>T
ENST00000553681.5:c.549G>T	ENSP00000451327.1:p.Glu183Asp
ENST00000554813.5:n.615G>T
ENST00000555414.5:c.549G>T	ENSP00000451979.1:p.Glu183Asp
ENST00000555839.5:c.462G>T	ENSP00000452460.1:p.Glu154Asp
ENST00000557054.1:c.28-23G>T	ENSP00000452212.2:n.28-23G>T
ENST00000557159.5:n.1165G>T
ENST00000557365.1:n.629G>T
ENST00000557592.5:c.498G>T	ENSP00000451060.1:p.Glu166Asp
NM_001244249.1:c.549G>T	NP_001231178.1:p.Glu183Asp
NM_001641.3:c.549G>T	NP_001632.2:p.Glu183Asp
NM_080648.2:c.549G>T	NP_542379.1:p.Glu183Asp
NM_080649.2:c.549G>T	NP_542380.1:p.Glu183Asp
XM_005267581.3:c.549G>T	XP_005267638.1:p.Glu183Asp
XM_005267582.3:c.498G>T	XP_005267639.1:p.Glu166Asp
NM_001641.4:c.549G>T MANE Select	NP_001632.2:p.Glu183Asp
NM_001244249.2:c.549G>T	NP_001231178.1:p.Glu183Asp
NM_080648.3:c.549G>T	NP_542379.1:p.Glu183Asp
NM_080649.3:c.549G>T	NP_542380.1:p.Glu183Asp