Canonical Allele Identifier: CA288233235

Gene: ZNF287

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16551947T>C , CM000679.2:g.16551947T>C	GRCh38
NC_000017.10:g.16455261T>C , CM000679.1:g.16455261T>C	GRCh37
NC_000017.9:g.16395986T>C	NCBI36
NG_051652.1:g.22266A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020653.4:c.2195A>G MANE Select	NP_065704.2:p.Tyr732Cys
ENST00000395825.4:c.2195A>G MANE Select	ENSP00000379169.3:p.Tyr732Cys
NM_001346167.1:c.2195A>G	NP_001333096.1:p.Tyr732Cys
NM_001346167.2:c.2195A>G	NP_001333096.1:p.Tyr732Cys
NM_001346168.1:c.2195A>G	NP_001333097.1:p.Tyr732Cys
NM_001346168.2:c.2195A>G	NP_001333097.1:p.Tyr732Cys
NM_001346169.1:c.2195A>G	NP_001333098.1:p.Tyr732Cys
NM_001346169.2:c.2195A>G	NP_001333098.1:p.Tyr732Cys
NM_001346170.1:c.2051A>G	NP_001333099.1:p.Tyr684Cys
NM_001346171.1:c.1688A>G	NP_001333100.1:p.Tyr563Cys
NM_001346171.2:c.1688A>G	NP_001333100.1:p.Tyr563Cys
NM_020653.2:c.2195A>G	NP_065704.2:p.Tyr732Cys
NM_020653.3:c.2195A>G	NP_065704.2:p.Tyr732Cys
ENST00000395824.5:c.2195A>G	ENSP00000379168.1:p.Tyr732Cys
ENST00000395825.3:c.2195A>G	ENSP00000379169.3:p.Tyr732Cys
XM_011523968.1:c.2195A>G	XP_011522270.1:p.Tyr732Cys
XM_011523968.2:c.2195A>G	XP_011522270.1:p.Tyr732Cys
XM_011523969.1:c.2195A>G	XP_011522271.1:p.Tyr732Cys
XR_001753080.2:n.368-3530T>C