Canonical Allele Identifier: CA1821826554
Gene: ZFAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.134610608G= , CM000670.2:g.134610608G= GRCh38
NC_000008.10:g.135622851G= , CM000670.1:g.135622851G= GRCh37
NC_000008.9:g.135692033G= NCBI36
NG_016356.1:g.107442C=
NG_016356.2:g.107442C=

Transcript Alleles

HGVS Amino-acid Change
NM_020863.4:c.496C= MANE Select NP_065914.2:p.Arg166=
ENST00000377838.8:c.496C= MANE Select ENSP00000367069.3:p.Arg166=
NM_001029939.3:c.460C= NP_001025110.2:p.Arg154=
NM_001029939.4:c.460C= NP_001025110.2:p.Arg154=
NM_001167583.2:c.460C= NP_001161055.1:p.Arg154=
NM_001167583.3:c.460C= NP_001161055.1:p.Arg154=
NM_001174157.1:c.449-1729C= NP_001167628.1:n.449-1729C=
NM_001174157.2:c.449-1729C= NP_001167628.1:n.449-1729C=
NM_001174158.1:c.460C= NP_001167629.1:p.Arg154=
NM_001174158.2:c.460C= NP_001167629.1:p.Arg154=
NM_001289394.1:c.460C= NP_001276323.1:p.Arg154=
NM_001289394.2:c.460C= NP_001276323.1:p.Arg154=
NM_020863.3:c.496C= NP_065914.2:p.Arg166=
NR_110323.1:n.682C=
NR_110323.2:n.664C=
ENST00000377838.7:c.496C= ENSP00000367069.3:p.Arg166=
ENST00000429442.6:c.460C= ENSP00000394501.2:p.Arg154=
ENST00000518191.1:c.413-1729C= ENSP00000428192.1:n.413-1729C=
ENST00000520214.5:c.460C= ENSP00000428483.1:p.Arg154=
ENST00000520356.5:c.460C= ENSP00000427879.1:p.Arg154=
ENST00000520727.5:c.460C= ENSP00000427831.1:p.Arg154=
ENST00000522257.5:c.310C= ENSP00000429983.1:p.Arg104=
ENST00000522974.5:n.601C=
ENST00000523040.1:n.181C=
ENST00000523243.5:c.496C= ENSP00000429930.1:p.Arg166=
ENST00000523399.5:c.449-1729C= ENSP00000429091.1:n.449-1729C=
ENST00000523924.5:c.*478C= ENSP00000429050.1:n.*478C=
XM_011517203.1:c.460C= XP_011515505.1:p.Arg154=
XM_011517204.1:c.310C= XP_011515506.1:p.Arg104=
XM_011517204.2:c.310C= XP_011515506.1:p.Arg104=
XM_011517205.1:c.460C= XP_011515507.1:p.Arg154=
XM_011517206.1:c.460C= XP_011515508.1:p.Arg154=
XM_011517206.2:c.460C= XP_011515508.1:p.Arg154=
XM_017013716.1:c.460C= XP_016869205.1:p.Arg154=
XR_001745568.1:n.477C=
XR_001745569.1:n.477C=
XR_001745570.1:n.477C=
XR_928343.1:n.477C=
XR_928343.2:n.477C=