Canonical Allele Identifier: CA2122040079

Gene: APEX1

Linked Data

• dbSNP Id: rs1881332941

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20456168T>C , CM000676.2:g.20456168T>C	GRCh38
NC_000014.8:g.20924327T>C , CM000676.1:g.20924327T>C	GRCh37
NC_000014.7:g.19994167T>C	NCBI36
NG_008718.1:g.6038T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000216714.8:c.246+67T>C MANE Select	ENSP00000216714.3:n.246+67T>C
ENST00000216714.7:c.246+67T>C	ENSP00000216714.3:n.246+67T>C
ENST00000398030.8:c.246+67T>C	ENSP00000381111.4:n.246+67T>C
ENST00000438886.1:c.95+67T>C
ENST00000553555.5:n.666+67T>C
ENST00000553681.5:c.246+67T>C	ENSP00000451327.1:n.246+67T>C
ENST00000554325.1:c.*166+67T>C	ENSP00000450604.1:n.*166+67T>C
ENST00000554813.5:n.312+67T>C
ENST00000555306.5:n.693+67T>C
ENST00000555414.5:c.246+67T>C	ENSP00000451979.1:n.246+67T>C
ENST00000555839.5:c.246+67T>C	ENSP00000452460.1:n.246+67T>C
ENST00000556054.5:c.246+67T>C	ENSP00000451170.1:n.246+67T>C
ENST00000557054.1:c.27+496T>C	ENSP00000452212.2:n.27+496T>C
ENST00000557150.5:c.195+67T>C	ENSP00000452418.1:n.195+67T>C
ENST00000557159.5:n.862+67T>C
ENST00000557181.5:c.246+67T>C	ENSP00000452304.1:n.246+67T>C
ENST00000557344.5:c.246+67T>C	ENSP00000452137.1:n.246+67T>C
ENST00000557365.1:n.326+67T>C
ENST00000557592.5:c.195+67T>C	ENSP00000451060.1:n.195+67T>C
NM_001244249.1:c.246+67T>C	NP_001231178.1:n.246+67T>C
NM_001641.3:c.246+67T>C	NP_001632.2:n.246+67T>C
NM_080648.2:c.246+67T>C	NP_542379.1:n.246+67T>C
NM_080649.2:c.246+67T>C	NP_542380.1:n.246+67T>C
XM_005267581.3:c.246+67T>C	XP_005267638.1:n.246+67T>C
XM_005267582.3:c.195+67T>C	XP_005267639.1:n.195+67T>C
NM_001641.4:c.246+67T>C MANE Select	NP_001632.2:n.246+67T>C
NM_001244249.2:c.246+67T>C	NP_001231178.1:n.246+67T>C
NM_080648.3:c.246+67T>C	NP_542379.1:n.246+67T>C
NM_080649.3:c.246+67T>C	NP_542380.1:n.246+67T>C