Canonical Allele Identifier: CA485450281

Gene: APEX1

Linked Data

• MyVariant Identifiers: chr14:g.20924985C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20456826C>G , CM000676.2:g.20456826C>G	GRCh38
NC_000014.8:g.20924985C>G , CM000676.1:g.20924985C>G	GRCh37
NC_000014.7:g.19994825C>G	NCBI36
NG_008718.1:g.6696C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216714.8:c.405C>G MANE Select	ENSP00000216714.3:p.Ser135=
ENST00000216714.7:c.405C>G	ENSP00000216714.3:p.Ser135=
ENST00000398030.8:c.405C>G	ENSP00000381111.4:p.Ser135=
ENST00000438886.1:c.254C>G
ENST00000553555.5:n.825C>G
ENST00000553681.5:c.405C>G	ENSP00000451327.1:p.Ser135=
ENST00000554813.5:n.471C>G
ENST00000555306.5:n.852C>G
ENST00000555414.5:c.405C>G	ENSP00000451979.1:p.Ser135=
ENST00000555839.5:c.405C>G	ENSP00000452460.1:p.Ser135=
ENST00000556054.5:c.405C>G	ENSP00000451170.1:p.Ser135=
ENST00000557054.1:c.28-297C>G	ENSP00000452212.2:n.28-297C>G
ENST00000557150.5:c.354C>G	ENSP00000452418.1:p.Ser118=
ENST00000557159.5:n.1021C>G
ENST00000557344.5:c.405C>G	ENSP00000452137.1:p.Ser135=
ENST00000557365.1:n.485C>G
ENST00000557592.5:c.354C>G	ENSP00000451060.1:p.Ser118=
NM_001244249.1:c.405C>G	NP_001231178.1:p.Ser135=
NM_001641.3:c.405C>G	NP_001632.2:p.Ser135=
NM_080648.2:c.405C>G	NP_542379.1:p.Ser135=
NM_080649.2:c.405C>G	NP_542380.1:p.Ser135=
XM_005267581.3:c.405C>G	XP_005267638.1:p.Ser135=
XM_005267582.3:c.354C>G	XP_005267639.1:p.Ser118=
NM_001641.4:c.405C>G MANE Select	NP_001632.2:p.Ser135=
NM_001244249.2:c.405C>G	NP_001231178.1:p.Ser135=
NM_080648.3:c.405C>G	NP_542379.1:p.Ser135=
NM_080649.3:c.405C>G	NP_542380.1:p.Ser135=