Canonical Allele Identifier: CA376295356

Gene: ZNF33A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.38055293G>T , CM000672.2:g.38055293G>T	GRCh38
NC_000010.10:g.38344221G>T , CM000672.1:g.38344221G>T	GRCh37
NC_000010.9:g.38384227G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006954.2:c.1169G>T MANE Select	NP_008885.1:p.Cys390Phe
ENST00000432900.7:c.1169G>T MANE Select	ENSP00000402467.3:p.Cys390Phe
NM_001278170.1:c.1187G>T	NP_001265099.1:p.Cys396Phe
NM_001278170.2:c.1187G>T	NP_001265099.1:p.Cys396Phe
NM_001278171.1:c.833G>T	NP_001265100.1:p.Cys278Phe
NM_001278171.2:c.833G>T	NP_001265100.1:p.Cys278Phe
NM_001278173.1:c.1223G>T	NP_001265102.1:p.Cys408Phe
NM_001278174.1:c.833G>T	NP_001265103.1:p.Cys278Phe
NM_001278174.2:c.833G>T	NP_001265103.1:p.Cys278Phe
NM_001278175.1:c.935G>T	NP_001265104.1:p.Cys312Phe
NM_001278175.2:c.935G>T	NP_001265104.1:p.Cys312Phe
NM_001278176.1:c.1040G>T	NP_001265105.1:p.Cys347Phe
NM_001278176.2:c.1040G>T	NP_001265105.1:p.Cys347Phe
NM_001278177.1:c.1232G>T	NP_001265106.1:p.Cys411Phe
NM_001278177.2:c.1232G>T	NP_001265106.1:p.Cys411Phe
NM_001278178.1:c.833G>T	NP_001265107.1:p.Cys278Phe
NM_001278179.1:c.833G>T	NP_001265108.1:p.Cys278Phe
NM_001278179.2:c.833G>T	NP_001265108.1:p.Cys278Phe
NM_001324175.1:c.833G>T	NP_001311104.1:p.Cys278Phe
NM_001324175.2:c.833G>T	NP_001311104.1:p.Cys278Phe
NM_001324176.1:c.833G>T	NP_001311105.1:p.Cys278Phe
NM_001324176.2:c.833G>T	NP_001311105.1:p.Cys278Phe
NM_001324177.1:c.833G>T	NP_001311106.1:p.Cys278Phe
NM_001324177.2:c.833G>T	NP_001311106.1:p.Cys278Phe
NM_001324178.1:c.1190G>T	NP_001311107.1:p.Cys397Phe
NM_001324178.2:c.1190G>T	NP_001311107.1:p.Cys397Phe
NM_006954.1:c.1169G>T	NP_008885.1:p.Cys390Phe
NM_006974.2:c.1166G>T	NP_008905.1:p.Cys389Phe
NM_006974.3:c.1166G>T	NP_008905.1:p.Cys389Phe
NR_136709.1:n.533+814G>T
NR_136709.2:n.508+814G>T
NR_136710.1:n.429-8795G>T
NR_136710.2:n.404-8795G>T
ENST00000307441.13:c.1223G>T	ENSP00000304268.10:p.Cys408Phe
ENST00000374618.7:c.833G>T	ENSP00000363747.4:p.Cys278Phe
ENST00000432900.6:c.1169G>T	ENSP00000402467.3:p.Cys390Phe
ENST00000458705.6:c.1166G>T	ENSP00000387713.2:p.Cys389Phe
ENST00000469037.2:c.387+782G>T	ENSP00000437022.1:n.387+782G>T
ENST00000628825.2:c.1187G>T	ENSP00000485869.1:p.Cys396Phe
XM_011519650.1:c.1169G>T	XP_011517952.1:p.Cys390Phe
XM_011519650.2:c.1169G>T	XP_011517952.1:p.Cys390Phe
XM_011519651.1:c.1166G>T	XP_011517953.1:p.Cys389Phe
XM_011519651.2:c.1166G>T	XP_011517953.1:p.Cys389Phe
XM_011519652.1:c.1238G>T	XP_011517954.1:p.Cys413Phe
XM_011519653.1:c.935G>T	XP_011517955.1:p.Cys312Phe
XM_011519653.2:c.935G>T	XP_011517955.1:p.Cys312Phe
XM_011519654.1:c.932G>T	XP_011517956.1:p.Cys311Phe
XM_011519654.2:c.932G>T	XP_011517956.1:p.Cys311Phe
XM_017016617.1:c.1190G>T	XP_016872106.1:p.Cys397Phe