Canonical Allele Identifier: CA485450217

Gene: APEX1

Linked Data

• MyVariant Identifiers: chr14:g.20925421C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20457262C>G , CM000676.2:g.20457262C>G	GRCh38
NC_000014.8:g.20925421C>G , CM000676.1:g.20925421C>G	GRCh37
NC_000014.7:g.19995261C>G	NCBI36
NG_008718.1:g.7132C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216714.8:c.711C>G MANE Select	ENSP00000216714.3:p.Arg237=
ENST00000216714.7:c.711C>G	ENSP00000216714.3:p.Arg237=
ENST00000398030.8:c.711C>G	ENSP00000381111.4:p.Arg237=
ENST00000553555.5:n.1131C>G
ENST00000553681.5:c.711C>G	ENSP00000451327.1:p.Arg237=
ENST00000555414.5:c.711C>G	ENSP00000451979.1:p.Arg237=
ENST00000555839.5:c.624C>G	ENSP00000452460.1:p.Arg208=
ENST00000557054.1:c.*122C>G	ENSP00000452212.2:n.*122C>G
ENST00000557159.5:n.1327C>G
ENST00000557365.1:n.791C>G
NM_001244249.1:c.711C>G	NP_001231178.1:p.Arg237=
NM_001641.3:c.711C>G	NP_001632.2:p.Arg237=
NM_080648.2:c.711C>G	NP_542379.1:p.Arg237=
NM_080649.2:c.711C>G	NP_542380.1:p.Arg237=
XM_005267581.3:c.711C>G	XP_005267638.1:p.Arg237=
XM_005267582.3:c.660C>G	XP_005267639.1:p.Arg220=
NM_001641.4:c.711C>G MANE Select	NP_001632.2:p.Arg237=
NM_001244249.2:c.711C>G	NP_001231178.1:p.Arg237=
NM_080648.3:c.711C>G	NP_542379.1:p.Arg237=
NM_080649.3:c.711C>G	NP_542380.1:p.Arg237=