Canonical Allele Identifier: CA463219292
Gene: ZFAT HGNC NCBI

Linked Data

dbSNP Id: rs1292731437

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.134602309G>T , CM000670.2:g.134602309G>T GRCh38
NC_000008.10:g.135614552G>T , CM000670.1:g.135614552G>T GRCh37
NC_000008.9:g.135683734G>T NCBI36
NG_016356.1:g.115741C>A
NG_016356.2:g.115741C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377838.8:c.1410C>A MANE Select ENSP00000367069.3:p.Ser470=
ENST00000377838.7:c.1410C>A ENSP00000367069.3:p.Ser470=
ENST00000429442.6:c.1374C>A ENSP00000394501.2:p.Ser458=
ENST00000520214.5:c.1374C>A ENSP00000428483.1:p.Ser458=
ENST00000520356.5:c.1374C>A ENSP00000427879.1:p.Ser458=
ENST00000520727.5:c.1374C>A ENSP00000427831.1:p.Ser458=
ENST00000522974.5:n.1515C>A
ENST00000523243.5:c.1410C>A ENSP00000429930.1:p.Ser470=
ENST00000523399.5:c.1224C>A ENSP00000429091.1:p.Ser408=
ENST00000523924.5:c.*1392C>A ENSP00000429050.1:n.*1392C>A
NM_001029939.3:c.1374C>A NP_001025110.2:p.Ser458=
NM_001167583.2:c.1374C>A NP_001161055.1:p.Ser458=
NM_001174157.1:c.1224C>A NP_001167628.1:p.Ser408=
NM_001174158.1:c.1374C>A NP_001167629.1:p.Ser458=
NM_001289394.1:c.1374C>A NP_001276323.1:p.Ser458=
NM_020863.3:c.1410C>A NP_065914.2:p.Ser470=
NR_110323.1:n.1596C>A
XM_011517203.1:c.1374C>A XP_011515505.1:p.Ser458=
XM_011517204.1:c.1224C>A XP_011515506.1:p.Ser408=
XM_011517205.1:c.1374C>A XP_011515507.1:p.Ser458=
XM_011517206.1:c.1374C>A XP_011515508.1:p.Ser458=
XR_928343.1:n.1391C>A
XM_011517204.2:c.1224C>A XP_011515506.1:p.Ser408=
XM_011517206.2:c.1374C>A XP_011515508.1:p.Ser458=
XM_017013716.1:c.1374C>A XP_016869205.1:p.Ser458=
XR_001745568.1:n.1391C>A
XR_001745569.1:n.1391C>A
XR_001745570.1:n.1391C>A
XR_928343.2:n.1391C>A
NM_020863.4:c.1410C>A MANE Select NP_065914.2:p.Ser470=
NM_001029939.4:c.1374C>A NP_001025110.2:p.Ser458=
NM_001167583.3:c.1374C>A NP_001161055.1:p.Ser458=
NM_001174157.2:c.1224C>A NP_001167628.1:p.Ser408=
NM_001174158.2:c.1374C>A NP_001167629.1:p.Ser458=
NM_001289394.2:c.1374C>A NP_001276323.1:p.Ser458=
NR_110323.2:n.1578C>A