Canonical Allele Identifier: CA12799286
Gene: ZFAT HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11166629

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.134624721C>T , CM000670.2:g.134624721C>T GRCh38
NC_000008.10:g.135636964C>T , CM000670.1:g.135636964C>T GRCh37
NC_000008.9:g.135706146C>T NCBI36
NG_016356.1:g.93329G>A
NG_016356.2:g.93329G>A

Transcript Alleles

HGVS Amino-acid change
NM_001029939.3:c.412+12740G>A VV NP_001025110.2:p.=
NM_001167583.2:c.412+12740G>A VV NP_001161055.1:p.=
NM_001174157.1:c.448+12740G>A VV NP_001167628.1:p.=
NM_001174158.1:c.412+12740G>A VV NP_001167629.1:p.=
NM_001289394.1:c.412+12740G>A VV NP_001276323.1:p.=
NM_020863.3:c.448+12740G>A VV NP_065914.2:p.=
NR_110323.1:n.634+12740G>A
XM_011517203.1:c.412+12740G>A XP_011515505.1:p.=
XM_011517204.1:c.262+12740G>A XP_011515506.1:p.=
XM_011517205.1:c.412+12740G>A XP_011515507.1:p.=
XM_011517206.1:c.412+12740G>A XP_011515508.1:p.=
XR_928343.1:n.429+12740G>A
XM_011517204.2:c.262+12740G>A XP_011515506.1:p.=
XM_011517206.2:c.412+12740G>A XP_011515508.1:p.=
XM_017013716.1:c.412+12740G>A XP_016869205.1:p.=
XR_001745568.1:n.429+12740G>A
XR_001745569.1:n.429+12740G>A
XR_001745570.1:n.429+12740G>A
XR_928343.2:n.429+12740G>A
NM_020863.4:c.448+12740G>A VV MANE Preferred NP_065914.2:p.=
ENST00000377838.7:c.448+12740G>A ENSP00000367069.3:p.=
ENST00000429442.6:c.412+12740G>A ENSP00000394501.2:p.=
ENST00000518191.1:c.412+12740G>A ENSP00000428192.1:p.=
ENST00000520214.5:c.412+12740G>A ENSP00000428483.1:p.=
ENST00000520356.5:c.412+12740G>A ENSP00000427879.1:p.=
ENST00000520727.5:c.412+12740G>A ENSP00000427831.1:p.=
ENST00000522257.5:c.262+12740G>A ENSP00000429983.1:p.=
ENST00000522974.5:n.553+12740G>A
ENST00000523040.1:n.133+12740G>A
ENST00000523243.5:c.448+12740G>A ENSP00000429930.1:p.=
ENST00000523399.5:c.448+12740G>A ENSP00000429091.1:p.=
ENST00000523924.5:c.*430+12740G>A ENSP00000429050.1:p.=