Canonical Allele Identifier: CA485449940

Gene: APEX1

Linked Data

• MyVariant Identifiers: chr14:g.20925364T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20457205T>A , CM000676.2:g.20457205T>A	GRCh38
NC_000014.8:g.20925364T>A , CM000676.1:g.20925364T>A	GRCh37
NC_000014.7:g.19995204T>A	NCBI36
NG_008718.1:g.7075T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216714.8:c.654T>A MANE Select	ENSP00000216714.3:p.Ile218=
ENST00000216714.7:c.654T>A	ENSP00000216714.3:p.Ile218=
ENST00000398030.8:c.654T>A	ENSP00000381111.4:p.Ile218=
ENST00000438886.1:c.434T>A
ENST00000553555.5:n.1074T>A
ENST00000553681.5:c.654T>A	ENSP00000451327.1:p.Ile218=
ENST00000555414.5:c.654T>A	ENSP00000451979.1:p.Ile218=
ENST00000555839.5:c.567T>A	ENSP00000452460.1:p.Ile189=
ENST00000557054.1:c.*65T>A	ENSP00000452212.2:n.*65T>A
ENST00000557159.5:n.1270T>A
ENST00000557365.1:n.734T>A
NM_001244249.1:c.654T>A	NP_001231178.1:p.Ile218=
NM_001641.3:c.654T>A	NP_001632.2:p.Ile218=
NM_080648.2:c.654T>A	NP_542379.1:p.Ile218=
NM_080649.2:c.654T>A	NP_542380.1:p.Ile218=
XM_005267581.3:c.654T>A	XP_005267638.1:p.Ile218=
XM_005267582.3:c.603T>A	XP_005267639.1:p.Ile201=
NM_001641.4:c.654T>A MANE Select	NP_001632.2:p.Ile218=
NM_001244249.2:c.654T>A	NP_001231178.1:p.Ile218=
NM_080648.3:c.654T>A	NP_542379.1:p.Ile218=
NM_080649.3:c.654T>A	NP_542380.1:p.Ile218=