Canonical Allele Identifier: CA612862189

Gene: APEX1

Linked Data

• dbSNP Id: rs1457493560
• gnomAD v2: 14-20924904-TC-T
• gnomAD v4: 14-20456745-TC-T
• MyVariant Identifiers: chr14:g.20924905del (hg19) ; chr14:g.20456746del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20456746del , CM000676.2:g.20456746del	GRCh38
NC_000014.8:g.20924905del , CM000676.1:g.20924905del	GRCh37
NC_000014.7:g.19994745del	NCBI36
NG_008718.1:g.6616del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216714.8:c.325del MANE Select	ENSP00000216714.3:p.Gln109ArgfsTer?
ENST00000216714.7:c.325del	ENSP00000216714.3:p.Gln109ArgfsTer?
ENST00000398030.8:c.325del	ENSP00000381111.4:p.Gln109ArgfsTer?
ENST00000438886.1:c.174del
ENST00000553555.5:n.745del
ENST00000553681.5:c.325del	ENSP00000451327.1:p.Gln109ArgfsTer?
ENST00000554813.5:n.391del
ENST00000555306.5:n.772del
ENST00000555414.5:c.325del	ENSP00000451979.1:p.Gln109ArgfsTer?
ENST00000555839.5:c.325del	ENSP00000452460.1:p.Gln109ArgfsTer?
ENST00000556054.5:c.325del	ENSP00000451170.1:p.Gln109ArgfsTer?
ENST00000557054.1:c.28-377del	ENSP00000452212.2:n.28-377del
ENST00000557150.5:c.274del	ENSP00000452418.1:p.Gln92ArgfsTer?
ENST00000557159.5:n.941del
ENST00000557344.5:c.325del	ENSP00000452137.1:p.Gln109ArgfsTer?
ENST00000557365.1:n.405del
ENST00000557592.5:c.274del	ENSP00000451060.1:p.Gln92ArgfsTer?
NM_001244249.1:c.325del	NP_001231178.1:p.Gln109ArgfsTer?
NM_001641.3:c.325del	NP_001632.2:p.Gln109ArgfsTer?
NM_080648.2:c.325del	NP_542379.1:p.Gln109ArgfsTer?
NM_080649.2:c.325del	NP_542380.1:p.Gln109ArgfsTer?
XM_005267581.3:c.325del	XP_005267638.1:p.Gln109ArgfsTer?
XM_005267582.3:c.274del	XP_005267639.1:p.Gln92ArgfsTer?
NM_001641.4:c.325del MANE Select	NP_001632.2:p.Gln109ArgfsTer?
NM_001244249.2:c.325del	NP_001231178.1:p.Gln109ArgfsTer?
NM_080648.3:c.325del	NP_542379.1:p.Gln109ArgfsTer?
NM_080649.3:c.325del	NP_542380.1:p.Gln109ArgfsTer?