Canonical Allele Identifier: CA389131766

Gene: APEX1

Linked Data

• MyVariant Identifiers: chr14:g.20925196T>G (hg19) ; chr14:g.20457037T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20457037T>G , CM000676.2:g.20457037T>G	GRCh38
NC_000014.8:g.20925196T>G , CM000676.1:g.20925196T>G	GRCh37
NC_000014.7:g.19995036T>G	NCBI36
NG_008718.1:g.6907T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216714.8:c.486T>G MANE Select	ENSP00000216714.3:p.Phe162Leu
ENST00000216714.7:c.486T>G	ENSP00000216714.3:p.Phe162Leu
ENST00000398030.8:c.486T>G	ENSP00000381111.4:p.Phe162Leu
ENST00000438886.1:c.289-23T>G
ENST00000553555.5:n.906T>G
ENST00000553681.5:c.486T>G	ENSP00000451327.1:p.Phe162Leu
ENST00000554813.5:n.552T>G
ENST00000555414.5:c.486T>G	ENSP00000451979.1:p.Phe162Leu
ENST00000555839.5:c.440-41T>G	ENSP00000452460.1:n.440-41T>G
ENST00000556054.5:c.486T>G	ENSP00000451170.1:p.Phe162Leu
ENST00000557054.1:c.28-86T>G	ENSP00000452212.2:n.28-86T>G
ENST00000557150.5:c.435T>G	ENSP00000452418.1:p.Phe145Leu
ENST00000557159.5:n.1102T>G
ENST00000557365.1:n.566T>G
ENST00000557592.5:c.435T>G	ENSP00000451060.1:p.Phe145Leu
NM_001244249.1:c.486T>G	NP_001231178.1:p.Phe162Leu
NM_001641.3:c.486T>G	NP_001632.2:p.Phe162Leu
NM_080648.2:c.486T>G	NP_542379.1:p.Phe162Leu
NM_080649.2:c.486T>G	NP_542380.1:p.Phe162Leu
XM_005267581.3:c.486T>G	XP_005267638.1:p.Phe162Leu
XM_005267582.3:c.435T>G	XP_005267639.1:p.Phe145Leu
NM_001641.4:c.486T>G MANE Select	NP_001632.2:p.Phe162Leu
NM_001244249.2:c.486T>G	NP_001231178.1:p.Phe162Leu
NM_080648.3:c.486T>G	NP_542379.1:p.Phe162Leu
NM_080649.3:c.486T>G	NP_542380.1:p.Phe162Leu