Canonical Allele Identifier: CA1821821442

Gene: ZFAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.134602358T= , CM000670.2:g.134602358T=	GRCh38
NC_000008.10:g.135614601T= , CM000670.1:g.135614601T=	GRCh37
NC_000008.9:g.135683783T=	NCBI36
NG_016356.1:g.115692A=
NG_016356.2:g.115692A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377838.8:c.1361A= MANE Select	ENSP00000367069.3:p.His454=
ENST00000377838.7:c.1361A=	ENSP00000367069.3:p.His454=
ENST00000429442.6:c.1325A=	ENSP00000394501.2:p.His442=
ENST00000520214.5:c.1325A=	ENSP00000428483.1:p.His442=
ENST00000520356.5:c.1325A=	ENSP00000427879.1:p.His442=
ENST00000520727.5:c.1325A=	ENSP00000427831.1:p.His442=
ENST00000522974.5:n.1466A=
ENST00000523243.5:c.1361A=	ENSP00000429930.1:p.His454=
ENST00000523399.5:c.1175A=	ENSP00000429091.1:p.His392=
ENST00000523924.5:c.*1343A=	ENSP00000429050.1:n.*1343A=
NM_001029939.3:c.1325A=	NP_001025110.2:p.His442=
NM_001167583.2:c.1325A=	NP_001161055.1:p.His442=
NM_001174157.1:c.1175A=	NP_001167628.1:p.His392=
NM_001174158.1:c.1325A=	NP_001167629.1:p.His442=
NM_001289394.1:c.1325A=	NP_001276323.1:p.His442=
NM_020863.3:c.1361A=	NP_065914.2:p.His454=
NR_110323.1:n.1547A=
XM_011517203.1:c.1325A=	XP_011515505.1:p.His442=
XM_011517204.1:c.1175A=	XP_011515506.1:p.His392=
XM_011517205.1:c.1325A=	XP_011515507.1:p.His442=
XM_011517206.1:c.1325A=	XP_011515508.1:p.His442=
XR_928343.1:n.1342A=
XM_011517204.2:c.1175A=	XP_011515506.1:p.His392=
XM_011517206.2:c.1325A=	XP_011515508.1:p.His442=
XM_017013716.1:c.1325A=	XP_016869205.1:p.His442=
XR_001745568.1:n.1342A=
XR_001745569.1:n.1342A=
XR_001745570.1:n.1342A=
XR_928343.2:n.1342A=
NM_020863.4:c.1361A= MANE Select	NP_065914.2:p.His454=
NM_001029939.4:c.1325A=	NP_001025110.2:p.His442=
NM_001167583.3:c.1325A=	NP_001161055.1:p.His442=
NM_001174157.2:c.1175A=	NP_001167628.1:p.His392=
NM_001174158.2:c.1325A=	NP_001167629.1:p.His442=
NM_001289394.2:c.1325A=	NP_001276323.1:p.His442=
NR_110323.2:n.1529A=