Canonical Allele Identifier: CA2122041416

Gene: APEX1

Linked Data

• dbSNP Id: rs1881411637

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20456965A>G , CM000676.2:g.20456965A>G	GRCh38
NC_000014.8:g.20925124A>G , CM000676.1:g.20925124A>G	GRCh37
NC_000014.7:g.19994964A>G	NCBI36
NG_008718.1:g.6835A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216714.8:c.440-26A>G MANE Select	ENSP00000216714.3:n.440-26A>G
ENST00000216714.7:c.440-26A>G	ENSP00000216714.3:n.440-26A>G
ENST00000398030.8:c.440-26A>G	ENSP00000381111.4:n.440-26A>G
ENST00000438886.1:c.289-95A>G
ENST00000553555.5:n.860-26A>G
ENST00000553681.5:c.440-26A>G	ENSP00000451327.1:n.440-26A>G
ENST00000554813.5:n.506-26A>G
ENST00000555306.5:n.887-26A>G
ENST00000555414.5:c.440-26A>G	ENSP00000451979.1:n.440-26A>G
ENST00000555839.5:c.439+105A>G	ENSP00000452460.1:n.439+105A>G
ENST00000556054.5:c.440-26A>G	ENSP00000451170.1:n.440-26A>G
ENST00000557054.1:c.28-158A>G	ENSP00000452212.2:n.28-158A>G
ENST00000557150.5:c.389-26A>G	ENSP00000452418.1:n.389-26A>G
ENST00000557159.5:n.1056-26A>G
ENST00000557365.1:n.520-26A>G
ENST00000557592.5:c.389-26A>G	ENSP00000451060.1:n.389-26A>G
NM_001244249.1:c.440-26A>G	NP_001231178.1:n.440-26A>G
NM_001641.3:c.440-26A>G	NP_001632.2:n.440-26A>G
NM_080648.2:c.440-26A>G	NP_542379.1:n.440-26A>G
NM_080649.2:c.440-26A>G	NP_542380.1:n.440-26A>G
XM_005267581.3:c.440-26A>G	XP_005267638.1:n.440-26A>G
XM_005267582.3:c.389-26A>G	XP_005267639.1:n.389-26A>G
NM_001641.4:c.440-26A>G MANE Select	NP_001632.2:n.440-26A>G
NM_001244249.2:c.440-26A>G	NP_001231178.1:n.440-26A>G
NM_080648.3:c.440-26A>G	NP_542379.1:n.440-26A>G
NM_080649.3:c.440-26A>G	NP_542380.1:n.440-26A>G