Canonical Allele Identifier: CA1821821245

Gene: ZFAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.134602249G= , CM000670.2:g.134602249G=	GRCh38
NC_000008.10:g.135614492G= , CM000670.1:g.135614492G=	GRCh37
NC_000008.9:g.135683674G=	NCBI36
NG_016356.1:g.115801C=
NG_016356.2:g.115801C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377838.8:c.1470C= MANE Select	ENSP00000367069.3:p.Phe490=
ENST00000377838.7:c.1470C=	ENSP00000367069.3:p.Phe490=
ENST00000429442.6:c.1434C=	ENSP00000394501.2:p.Phe478=
ENST00000520214.5:c.1434C=	ENSP00000428483.1:p.Phe478=
ENST00000520356.5:c.1434C=	ENSP00000427879.1:p.Phe478=
ENST00000520727.5:c.1434C=	ENSP00000427831.1:p.Phe478=
ENST00000522974.5:n.1575C=
ENST00000523243.5:c.1470C=	ENSP00000429930.1:p.Phe490=
ENST00000523399.5:c.1284C=	ENSP00000429091.1:p.Phe428=
ENST00000523924.5:c.*1452C=	ENSP00000429050.1:n.*1452C=
NM_001029939.3:c.1434C=	NP_001025110.2:p.Phe478=
NM_001167583.2:c.1434C=	NP_001161055.1:p.Phe478=
NM_001174157.1:c.1284C=	NP_001167628.1:p.Phe428=
NM_001174158.1:c.1434C=	NP_001167629.1:p.Phe478=
NM_001289394.1:c.1434C=	NP_001276323.1:p.Phe478=
NM_020863.3:c.1470C=	NP_065914.2:p.Phe490=
NR_110323.1:n.1656C=
XM_011517203.1:c.1434C=	XP_011515505.1:p.Phe478=
XM_011517204.1:c.1284C=	XP_011515506.1:p.Phe428=
XM_011517205.1:c.1434C=	XP_011515507.1:p.Phe478=
XM_011517206.1:c.1434C=	XP_011515508.1:p.Phe478=
XR_928343.1:n.1451C=
XM_011517204.2:c.1284C=	XP_011515506.1:p.Phe428=
XM_011517206.2:c.1434C=	XP_011515508.1:p.Phe478=
XM_017013716.1:c.1434C=	XP_016869205.1:p.Phe478=
XR_001745568.1:n.1451C=
XR_001745569.1:n.1451C=
XR_001745570.1:n.1451C=
XR_928343.2:n.1451C=
NM_020863.4:c.1470C= MANE Select	NP_065914.2:p.Phe490=
NM_001029939.4:c.1434C=	NP_001025110.2:p.Phe478=
NM_001167583.3:c.1434C=	NP_001161055.1:p.Phe478=
NM_001174157.2:c.1284C=	NP_001167628.1:p.Phe428=
NM_001174158.2:c.1434C=	NP_001167629.1:p.Phe478=
NM_001289394.2:c.1434C=	NP_001276323.1:p.Phe478=
NR_110323.2:n.1638C=