Canonical Allele Identifier: CA389133176

Gene: APEX1

Linked Data

• MyVariant Identifiers: chr14:g.20925424A>C (hg19) ; chr14:g.20457265A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20457265A>C , CM000676.2:g.20457265A>C	GRCh38
NC_000014.8:g.20925424A>C , CM000676.1:g.20925424A>C	GRCh37
NC_000014.7:g.19995264A>C	NCBI36
NG_008718.1:g.7135A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216714.8:c.714A>C MANE Select	ENSP00000216714.3:p.Gln238His
ENST00000216714.7:c.714A>C	ENSP00000216714.3:p.Gln238His
ENST00000398030.8:c.714A>C	ENSP00000381111.4:p.Gln238His
ENST00000553555.5:n.1134A>C
ENST00000553681.5:c.714A>C	ENSP00000451327.1:p.Gln238His
ENST00000555414.5:c.714A>C	ENSP00000451979.1:p.Gln238His
ENST00000555839.5:c.627A>C	ENSP00000452460.1:p.Gln209His
ENST00000557054.1:c.*125A>C	ENSP00000452212.2:n.*125A>C
ENST00000557159.5:n.1330A>C
ENST00000557365.1:n.794A>C
NM_001244249.1:c.714A>C	NP_001231178.1:p.Gln238His
NM_001641.3:c.714A>C	NP_001632.2:p.Gln238His
NM_080648.2:c.714A>C	NP_542379.1:p.Gln238His
NM_080649.2:c.714A>C	NP_542380.1:p.Gln238His
XM_005267581.3:c.714A>C	XP_005267638.1:p.Gln238His
XM_005267582.3:c.663A>C	XP_005267639.1:p.Gln221His
NM_001641.4:c.714A>C MANE Select	NP_001632.2:p.Gln238His
NM_001244249.2:c.714A>C	NP_001231178.1:p.Gln238His
NM_080648.3:c.714A>C	NP_542379.1:p.Gln238His
NM_080649.3:c.714A>C	NP_542380.1:p.Gln238His