Canonical Allele Identifier: CA1999672387

Gene: ZC3H12C RDX

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110125219C>G , CM000673.2:g.110125219C>G	GRCh38
NC_000011.9:g.109995944C>G , CM000673.1:g.109995944C>G	GRCh37
NC_000011.8:g.109501154C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278590.8:c.22-11444C>G (ZC3H12C) MANE Select	ENSP00000278590.3:n.22-11444C>G
ENST00000645527.1:c.*546-949G>C (RDX)	ENSP00000496121.1:n.*546-949G>C
ENST00000278590.7:c.22-11444C>G (ZC3H12C)	ENSP00000278590.3:n.22-11444C>G
NM_033390.1:c.22-11444C>G (ZC3H12C)	NP_203748.1:n.22-11444C>G
XM_005271715.2:c.25-11444C>G (ZC3H12C)	XP_005271772.1:n.25-11444C>G
XM_011543055.1:c.-72-11444C>G (ZC3H12C)	XP_011541357.1:n.-72-11444C>G
XM_011543056.1:c.-72-11444C>G (ZC3H12C)	XP_011541358.1:n.-72-11444C>G
XM_005271715.4:c.25-11444C>G (ZC3H12C)	XP_005271772.1:n.25-11444C>G
XM_011543055.2:c.-72-11444C>G (ZC3H12C)	XP_011541357.1:n.-72-11444C>G
NM_033390.2:c.22-11444C>G (ZC3H12C) MANE Select	NP_203748.1:n.22-11444C>G