Canonical Allele Identifier: CA1821821785

Gene: ZFAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.134602572T= , CM000670.2:g.134602572T=	GRCh38
NC_000008.10:g.135614815T= , CM000670.1:g.135614815T=	GRCh37
NC_000008.9:g.135683997T=	NCBI36
NG_016356.1:g.115478A=
NG_016356.2:g.115478A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377838.8:c.1147A= MANE Select	ENSP00000367069.3:p.Lys383=
ENST00000377838.7:c.1147A=	ENSP00000367069.3:p.Lys383=
ENST00000429442.6:c.1111A=	ENSP00000394501.2:p.Lys371=
ENST00000520214.5:c.1111A=	ENSP00000428483.1:p.Lys371=
ENST00000520356.5:c.1111A=	ENSP00000427879.1:p.Lys371=
ENST00000520727.5:c.1111A=	ENSP00000427831.1:p.Lys371=
ENST00000522974.5:n.1252A=
ENST00000523243.5:c.1147A=	ENSP00000429930.1:p.Lys383=
ENST00000523399.5:c.961A=	ENSP00000429091.1:p.Lys321=
ENST00000523924.5:c.*1129A=	ENSP00000429050.1:n.*1129A=
NM_001029939.3:c.1111A=	NP_001025110.2:p.Lys371=
NM_001167583.2:c.1111A=	NP_001161055.1:p.Lys371=
NM_001174157.1:c.961A=	NP_001167628.1:p.Lys321=
NM_001174158.1:c.1111A=	NP_001167629.1:p.Lys371=
NM_001289394.1:c.1111A=	NP_001276323.1:p.Lys371=
NM_020863.3:c.1147A=	NP_065914.2:p.Lys383=
NR_110323.1:n.1333A=
XM_011517203.1:c.1111A=	XP_011515505.1:p.Lys371=
XM_011517204.1:c.961A=	XP_011515506.1:p.Lys321=
XM_011517205.1:c.1111A=	XP_011515507.1:p.Lys371=
XM_011517206.1:c.1111A=	XP_011515508.1:p.Lys371=
XR_928343.1:n.1128A=
XM_011517204.2:c.961A=	XP_011515506.1:p.Lys321=
XM_011517206.2:c.1111A=	XP_011515508.1:p.Lys371=
XM_017013716.1:c.1111A=	XP_016869205.1:p.Lys371=
XR_001745568.1:n.1128A=
XR_001745569.1:n.1128A=
XR_001745570.1:n.1128A=
XR_928343.2:n.1128A=
NM_020863.4:c.1147A= MANE Select	NP_065914.2:p.Lys383=
NM_001029939.4:c.1111A=	NP_001025110.2:p.Lys371=
NM_001167583.3:c.1111A=	NP_001161055.1:p.Lys371=
NM_001174157.2:c.961A=	NP_001167628.1:p.Lys321=
NM_001174158.2:c.1111A=	NP_001167629.1:p.Lys371=
NM_001289394.2:c.1111A=	NP_001276323.1:p.Lys371=
NR_110323.2:n.1315A=