Canonical Allele Identifier: CA6334191

Gene: ZNF202

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123726283G>A , CM000673.2:g.123726283G>A	GRCh38
NC_000011.9:g.123596991G>A , CM000673.1:g.123596991G>A	GRCh37
NC_000011.8:g.123102201G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530393.6:c.1661C>T MANE Select	ENSP00000432504.1:p.Ala554Val
ENST00000336139.8:c.1661C>T	ENSP00000337724.4:p.Ala554Val
ENST00000529691.1:c.1661C>T	ENSP00000433881.1:p.Ala554Val
ENST00000530393.5:c.1661C>T	ENSP00000432504.1:p.Ala554Val
NM_001301779.1:c.1661C>T	NP_001288708.1:p.Ala554Val
NM_001301780.1:c.1661C>T	NP_001288709.1:p.Ala554Val
NM_001301819.1:c.989C>T	NP_001288748.1:p.Ala330Val
NM_003455.3:c.1661C>T	NP_003446.2:p.Ala554Val
XM_005271659.1:c.1661C>T	XP_005271716.1:p.Ala554Val
XM_005271660.1:c.1661C>T	XP_005271717.1:p.Ala554Val
XM_005271661.1:c.1661C>T	XP_005271718.1:p.Ala554Val
XM_005271664.1:c.989C>T	XP_005271721.1:p.Ala330Val
XM_006718901.2:c.1661C>T	XP_006718964.1:p.Ala554Val
XM_011542972.1:c.1661C>T	XP_011541274.1:p.Ala554Val
XM_011542973.1:c.1661C>T	XP_011541275.1:p.Ala554Val
XM_011542974.1:c.1661C>T	XP_011541276.1:p.Ala554Val
XM_011542975.1:c.1661C>T	XP_011541277.1:p.Ala554Val
XM_011542976.1:c.989C>T	XP_011541278.1:p.Ala330Val
XM_005271664.2:c.989C>T	XP_005271721.1:p.Ala330Val
XM_017018268.2:c.1661C>T	XP_016873757.1:p.Ala554Val
XM_024448682.1:c.989C>T	XP_024304450.1:p.Ala330Val
NM_003455.4:c.1661C>T MANE Select	NP_003446.2:p.Ala554Val
NM_001301779.2:c.1661C>T	NP_001288708.1:p.Ala554Val
NM_001301780.2:c.1661C>T	NP_001288709.1:p.Ala554Val