Canonical Allele Identifier: CA2122042156

Gene: APEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20457306G= , CM000676.2:g.20457306G=	GRCh38
NC_000014.8:g.20925465G= , CM000676.1:g.20925465G=	GRCh37
NC_000014.7:g.19995305G=	NCBI36
NG_008718.1:g.7176G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216714.8:c.755G= MANE Select	ENSP00000216714.3:p.Ser252=
ENST00000216714.7:c.755G=	ENSP00000216714.3:p.Ser252=
ENST00000398030.8:c.755G=	ENSP00000381111.4:p.Ser252=
ENST00000553555.5:n.1175G=
ENST00000553681.5:c.755G=	ENSP00000451327.1:p.Ser252=
ENST00000555414.5:c.755G=	ENSP00000451979.1:p.Ser252=
ENST00000555839.5:c.668G=	ENSP00000452460.1:p.Ser223=
ENST00000557054.1:c.*166G=	ENSP00000452212.2:n.*166G=
ENST00000557159.5:n.1371G=
NM_001244249.1:c.755G=	NP_001231178.1:p.Ser252=
NM_001641.3:c.755G=	NP_001632.2:p.Ser252=
NM_080648.2:c.755G=	NP_542379.1:p.Ser252=
NM_080649.2:c.755G=	NP_542380.1:p.Ser252=
XM_005267581.3:c.755G=	XP_005267638.1:p.Ser252=
XM_005267582.3:c.704G=	XP_005267639.1:p.Ser235=
NM_001641.4:c.755G= MANE Select	NP_001632.2:p.Ser252=
NM_001244249.2:c.755G=	NP_001231178.1:p.Ser252=
NM_080648.3:c.755G=	NP_542379.1:p.Ser252=
NM_080649.3:c.755G=	NP_542380.1:p.Ser252=