Canonical Allele Identifier: CA372080286
Gene: ZFAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.134602455G>C , CM000670.2:g.134602455G>C GRCh38
NC_000008.10:g.135614698G>C , CM000670.1:g.135614698G>C GRCh37
NC_000008.9:g.135683880G>C NCBI36
NG_016356.1:g.115595C>G
NG_016356.2:g.115595C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377838.8:c.1264C>G MANE Select ENSP00000367069.3:p.His422Asp
ENST00000377838.7:c.1264C>G ENSP00000367069.3:p.His422Asp
ENST00000429442.6:c.1228C>G ENSP00000394501.2:p.His410Asp
ENST00000520214.5:c.1228C>G ENSP00000428483.1:p.His410Asp
ENST00000520356.5:c.1228C>G ENSP00000427879.1:p.His410Asp
ENST00000520727.5:c.1228C>G ENSP00000427831.1:p.His410Asp
ENST00000522974.5:n.1369C>G
ENST00000523243.5:c.1264C>G ENSP00000429930.1:p.His422Asp
ENST00000523399.5:c.1078C>G ENSP00000429091.1:p.His360Asp
ENST00000523924.5:c.*1246C>G ENSP00000429050.1:n.*1246C>G
NM_001029939.3:c.1228C>G NP_001025110.2:p.His410Asp
NM_001167583.2:c.1228C>G NP_001161055.1:p.His410Asp
NM_001174157.1:c.1078C>G NP_001167628.1:p.His360Asp
NM_001174158.1:c.1228C>G NP_001167629.1:p.His410Asp
NM_001289394.1:c.1228C>G NP_001276323.1:p.His410Asp
NM_020863.3:c.1264C>G NP_065914.2:p.His422Asp
NR_110323.1:n.1450C>G
XM_011517203.1:c.1228C>G XP_011515505.1:p.His410Asp
XM_011517204.1:c.1078C>G XP_011515506.1:p.His360Asp
XM_011517205.1:c.1228C>G XP_011515507.1:p.His410Asp
XM_011517206.1:c.1228C>G XP_011515508.1:p.His410Asp
XR_928343.1:n.1245C>G
XM_011517204.2:c.1078C>G XP_011515506.1:p.His360Asp
XM_011517206.2:c.1228C>G XP_011515508.1:p.His410Asp
XM_017013716.1:c.1228C>G XP_016869205.1:p.His410Asp
XR_001745568.1:n.1245C>G
XR_001745569.1:n.1245C>G
XR_001745570.1:n.1245C>G
XR_928343.2:n.1245C>G
NM_020863.4:c.1264C>G MANE Select NP_065914.2:p.His422Asp
NM_001029939.4:c.1228C>G NP_001025110.2:p.His410Asp
NM_001167583.3:c.1228C>G NP_001161055.1:p.His410Asp
NM_001174157.2:c.1078C>G NP_001167628.1:p.His360Asp
NM_001174158.2:c.1228C>G NP_001167629.1:p.His410Asp
NM_001289394.2:c.1228C>G NP_001276323.1:p.His410Asp
NR_110323.2:n.1432C>G