Canonical Allele Identifier: CA485449887

Gene: APEX1

Linked Data

• dbSNP Id: rs1566514734
• gnomAD v2: 14-20925329-C-T
• gnomAD v4: 14-20457170-C-T
• MyVariant Identifiers: chr14:g.20925329C>T (hg19) ; chr14:g.20925329_20925331delinsTTG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20457170C>T , CM000676.2:g.20457170C>T	GRCh38
NC_000014.8:g.20925329C>T , CM000676.1:g.20925329C>T	GRCh37
NC_000014.7:g.19995169C>T	NCBI36
NG_008718.1:g.7040C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216714.8:c.619C>T MANE Select	ENSP00000216714.3:p.Leu207=
ENST00000216714.7:c.619C>T	ENSP00000216714.3:p.Leu207=
ENST00000398030.8:c.619C>T	ENSP00000381111.4:p.Leu207=
ENST00000438886.1:c.399C>T
ENST00000553555.5:n.1039C>T
ENST00000553681.5:c.619C>T	ENSP00000451327.1:p.Leu207=
ENST00000555414.5:c.619C>T	ENSP00000451979.1:p.Leu207=
ENST00000555839.5:c.532C>T	ENSP00000452460.1:p.Leu178=
ENST00000557054.1:c.*30C>T	ENSP00000452212.2:n.*30C>T
ENST00000557159.5:n.1235C>T
ENST00000557365.1:n.699C>T
NM_001244249.1:c.619C>T	NP_001231178.1:p.Leu207=
NM_001641.3:c.619C>T	NP_001632.2:p.Leu207=
NM_080648.2:c.619C>T	NP_542379.1:p.Leu207=
NM_080649.2:c.619C>T	NP_542380.1:p.Leu207=
XM_005267581.3:c.619C>T	XP_005267638.1:p.Leu207=
XM_005267582.3:c.568C>T	XP_005267639.1:p.Leu190=
NM_001641.4:c.619C>T MANE Select	NP_001632.2:p.Leu207=
NM_001244249.2:c.619C>T	NP_001231178.1:p.Leu207=
NM_080648.3:c.619C>T	NP_542379.1:p.Leu207=
NM_080649.3:c.619C>T	NP_542380.1:p.Leu207=