Canonical Allele Identifier: CA1821821550

Gene: ZFAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.134602426_134602427delinsAG , CM000670.2:g.134602426_134602427delinsAG	GRCh38
NC_000008.10:g.135614669_135614670delinsAG , CM000670.1:g.135614669_135614670delinsAG	GRCh37
NC_000008.9:g.135683851_135683852delinsAG	NCBI36
NG_016356.1:g.115623_115624delinsCT
NG_016356.2:g.115623_115624delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377838.8:c.1292_1293delinsCT MANE Select	ENSP00000367069.3:p.Pro431=
ENST00000377838.7:c.1292_1293delinsCT	ENSP00000367069.3:p.Pro431=
ENST00000429442.6:c.1256_1257delinsCT	ENSP00000394501.2:p.Pro419=
ENST00000520214.5:c.1256_1257delinsCT	ENSP00000428483.1:p.Pro419=
ENST00000520356.5:c.1256_1257delinsCT	ENSP00000427879.1:p.Pro419=
ENST00000520727.5:c.1256_1257delinsCT	ENSP00000427831.1:p.Pro419=
ENST00000522974.5:n.1397_1398delinsCT
ENST00000523243.5:c.1292_1293delinsCT	ENSP00000429930.1:p.Pro431=
ENST00000523399.5:c.1106_1107delinsCT	ENSP00000429091.1:p.Pro369=
ENST00000523924.5:c.*1274_*1275delinsCT	ENSP00000429050.1:n.*1274_*1275delinsCT
NM_001029939.3:c.1256_1257delinsCT	NP_001025110.2:p.Pro419=
NM_001167583.2:c.1256_1257delinsCT	NP_001161055.1:p.Pro419=
NM_001174157.1:c.1106_1107delinsCT	NP_001167628.1:p.Pro369=
NM_001174158.1:c.1256_1257delinsCT	NP_001167629.1:p.Pro419=
NM_001289394.1:c.1256_1257delinsCT	NP_001276323.1:p.Pro419=
NM_020863.3:c.1292_1293delinsCT	NP_065914.2:p.Pro431=
NR_110323.1:n.1478_1479delinsCT
XM_011517203.1:c.1256_1257delinsCT	XP_011515505.1:p.Pro419=
XM_011517204.1:c.1106_1107delinsCT	XP_011515506.1:p.Pro369=
XM_011517205.1:c.1256_1257delinsCT	XP_011515507.1:p.Pro419=
XM_011517206.1:c.1256_1257delinsCT	XP_011515508.1:p.Pro419=
XR_928343.1:n.1273_1274delinsCT
XM_011517204.2:c.1106_1107delinsCT	XP_011515506.1:p.Pro369=
XM_011517206.2:c.1256_1257delinsCT	XP_011515508.1:p.Pro419=
XM_017013716.1:c.1256_1257delinsCT	XP_016869205.1:p.Pro419=
XR_001745568.1:n.1273_1274delinsCT
XR_001745569.1:n.1273_1274delinsCT
XR_001745570.1:n.1273_1274delinsCT
XR_928343.2:n.1273_1274delinsCT
NM_020863.4:c.1292_1293delinsCT MANE Select	NP_065914.2:p.Pro431=
NM_001029939.4:c.1256_1257delinsCT	NP_001025110.2:p.Pro419=
NM_001167583.3:c.1256_1257delinsCT	NP_001161055.1:p.Pro419=
NM_001174157.2:c.1106_1107delinsCT	NP_001167628.1:p.Pro369=
NM_001174158.2:c.1256_1257delinsCT	NP_001167629.1:p.Pro419=
NM_001289394.2:c.1256_1257delinsCT	NP_001276323.1:p.Pro419=
NR_110323.2:n.1460_1461delinsCT