Canonical Allele Identifier: CA2122042075

Gene: APEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20457264A= , CM000676.2:g.20457264A=	GRCh38
NC_000014.8:g.20925423A= , CM000676.1:g.20925423A=	GRCh37
NC_000014.7:g.19995263A=	NCBI36
NG_008718.1:g.7134A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216714.8:c.713A= MANE Select	ENSP00000216714.3:p.Gln238=
ENST00000216714.7:c.713A=	ENSP00000216714.3:p.Gln238=
ENST00000398030.8:c.713A=	ENSP00000381111.4:p.Gln238=
ENST00000553555.5:n.1133A=
ENST00000553681.5:c.713A=	ENSP00000451327.1:p.Gln238=
ENST00000555414.5:c.713A=	ENSP00000451979.1:p.Gln238=
ENST00000555839.5:c.626A=	ENSP00000452460.1:p.Gln209=
ENST00000557054.1:c.*124A=	ENSP00000452212.2:n.*124A=
ENST00000557159.5:n.1329A=
ENST00000557365.1:n.793A=
NM_001244249.1:c.713A=	NP_001231178.1:p.Gln238=
NM_001641.3:c.713A=	NP_001632.2:p.Gln238=
NM_080648.2:c.713A=	NP_542379.1:p.Gln238=
NM_080649.2:c.713A=	NP_542380.1:p.Gln238=
XM_005267581.3:c.713A=	XP_005267638.1:p.Gln238=
XM_005267582.3:c.662A=	XP_005267639.1:p.Gln221=
NM_001641.4:c.713A= MANE Select	NP_001632.2:p.Gln238=
NM_001244249.2:c.713A=	NP_001231178.1:p.Gln238=
NM_080648.3:c.713A=	NP_542379.1:p.Gln238=
NM_080649.3:c.713A=	NP_542380.1:p.Gln238=