Canonical Allele Identifier: CA7081506

Gene: APEX1

Linked Data

• dbSNP Id: rs766820374
• ExAC: 14:20924853 A / C
• gnomAD v2: 14-20924853-A-C
• gnomAD v4: 14-20456694-A-C
• MyVariant Identifiers: chr14:g.20924853A>C (hg19) ; chr14:g.20456694A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20456694A>C , CM000676.2:g.20456694A>C	GRCh38
NC_000014.8:g.20924853A>C , CM000676.1:g.20924853A>C	GRCh37
NC_000014.7:g.19994693A>C	NCBI36
NG_008718.1:g.6564A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216714.8:c.273A>C MANE Select	ENSP00000216714.3:p.Ile91=
ENST00000216714.7:c.273A>C	ENSP00000216714.3:p.Ile91=
ENST00000398030.8:c.273A>C	ENSP00000381111.4:p.Ile91=
ENST00000438886.1:c.122A>C
ENST00000553555.5:n.693A>C
ENST00000553681.5:c.273A>C	ENSP00000451327.1:p.Ile91=
ENST00000554813.5:n.339A>C
ENST00000555306.5:n.720A>C
ENST00000555414.5:c.273A>C	ENSP00000451979.1:p.Ile91=
ENST00000555839.5:c.273A>C	ENSP00000452460.1:p.Ile91=
ENST00000556054.5:c.273A>C	ENSP00000451170.1:p.Ile91=
ENST00000557054.1:c.28-429A>C	ENSP00000452212.2:n.28-429A>C
ENST00000557150.5:c.222A>C	ENSP00000452418.1:p.Ile74=
ENST00000557159.5:n.889A>C
ENST00000557181.5:c.273A>C	ENSP00000452304.1:p.Ile91=
ENST00000557344.5:c.273A>C	ENSP00000452137.1:p.Ile91=
ENST00000557365.1:n.353A>C
ENST00000557592.5:c.222A>C	ENSP00000451060.1:p.Ile74=
NM_001244249.1:c.273A>C	NP_001231178.1:p.Ile91=
NM_001641.3:c.273A>C	NP_001632.2:p.Ile91=
NM_080648.2:c.273A>C	NP_542379.1:p.Ile91=
NM_080649.2:c.273A>C	NP_542380.1:p.Ile91=
XM_005267581.3:c.273A>C	XP_005267638.1:p.Ile91=
XM_005267582.3:c.222A>C	XP_005267639.1:p.Ile74=
NM_001641.4:c.273A>C MANE Select	NP_001632.2:p.Ile91=
NM_001244249.2:c.273A>C	NP_001231178.1:p.Ile91=
NM_080648.3:c.273A>C	NP_542379.1:p.Ile91=
NM_080649.3:c.273A>C	NP_542380.1:p.Ile91=