Canonical Allele Identifier: CA163195739

Gene: ZKSCAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100029943G>A , CM000669.2:g.100029943G>A	GRCh38
NC_000007.13:g.99627566G>A , CM000669.1:g.99627566G>A	GRCh37
NC_000007.12:g.99465502G>A	NCBI36
NG_051950.1:g.19392G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003439.4:c.663G>A MANE Select	NP_003430.1:p.Ala221=
ENST00000324306.11:c.663G>A MANE Select	ENSP00000323148.6:p.Ala221=
NM_001287054.1:c.555G>A	NP_001273983.1:p.Ala185=
NM_001287054.2:c.555G>A	NP_001273983.1:p.Ala185=
NM_001287054.3:c.555G>A	NP_001273983.1:p.Ala185=
NM_001287055.1:c.24G>A	NP_001273984.1:p.Ala8=
NM_001287055.2:c.24G>A	NP_001273984.1:p.Ala8=
NM_001287055.3:c.24G>A	NP_001273984.1:p.Ala8=
NM_001346579.1:c.663G>A	NP_001333508.1:p.Ala221=
NM_001346579.2:c.663G>A	NP_001333508.1:p.Ala221=
NM_001346580.1:c.555G>A	NP_001333509.1:p.Ala185=
NM_001346580.2:c.555G>A	NP_001333509.1:p.Ala185=
NM_001346581.1:c.663G>A	NP_001333510.1:p.Ala221=
NM_001346581.2:c.663G>A	NP_001333510.1:p.Ala221=
NM_003439.2:c.663G>A	NP_003430.1:p.Ala221=
NM_003439.3:c.663G>A	NP_003430.1:p.Ala221=
NR_144477.1:n.926G>A
NR_144477.2:n.882G>A
ENST00000324306.10:c.663G>A	ENSP00000323148.6:p.Ala221=
ENST00000426572.5:c.555G>A	ENSP00000409172.1:p.Ala185=
ENST00000535170.5:c.24G>A	ENSP00000443508.1:p.Ala8=
ENST00000620510.1:c.555G>A	ENSP00000480305.1:p.Ala185=
XM_005250565.3:c.663G>A	XP_005250622.1:p.Ala221=
XM_011516559.1:c.663G>A	XP_011514861.1:p.Ala221=
XM_011516559.3:c.663G>A	XP_011514861.1:p.Ala221=
XR_002956485.1:n.897G>A
XR_927529.1:n.897G>A
XR_927529.2:n.897G>A