Canonical Allele Identifier: CA463219151
Gene: ZFAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.135614477G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.134602234G>A , CM000670.2:g.134602234G>A GRCh38
NC_000008.10:g.135614477G>A , CM000670.1:g.135614477G>A GRCh37
NC_000008.9:g.135683659G>A NCBI36
NG_016356.1:g.115816C>T
NG_016356.2:g.115816C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377838.8:c.1485C>T MANE Select ENSP00000367069.3:p.Asn495=
ENST00000377838.7:c.1485C>T ENSP00000367069.3:p.Asn495=
ENST00000429442.6:c.1449C>T ENSP00000394501.2:p.Asn483=
ENST00000520214.5:c.1449C>T ENSP00000428483.1:p.Asn483=
ENST00000520356.5:c.1449C>T ENSP00000427879.1:p.Asn483=
ENST00000520727.5:c.1449C>T ENSP00000427831.1:p.Asn483=
ENST00000522974.5:n.1590C>T
ENST00000523243.5:c.1485C>T ENSP00000429930.1:p.Asn495=
ENST00000523399.5:c.1299C>T ENSP00000429091.1:p.Asn433=
ENST00000523924.5:c.*1467C>T ENSP00000429050.1:n.*1467C>T
NM_001029939.3:c.1449C>T NP_001025110.2:p.Asn483=
NM_001167583.2:c.1449C>T NP_001161055.1:p.Asn483=
NM_001174157.1:c.1299C>T NP_001167628.1:p.Asn433=
NM_001174158.1:c.1449C>T NP_001167629.1:p.Asn483=
NM_001289394.1:c.1449C>T NP_001276323.1:p.Asn483=
NM_020863.3:c.1485C>T NP_065914.2:p.Asn495=
NR_110323.1:n.1671C>T
XM_011517203.1:c.1449C>T XP_011515505.1:p.Asn483=
XM_011517204.1:c.1299C>T XP_011515506.1:p.Asn433=
XM_011517205.1:c.1449C>T XP_011515507.1:p.Asn483=
XM_011517206.1:c.1449C>T XP_011515508.1:p.Asn483=
XR_928343.1:n.1466C>T
XM_011517204.2:c.1299C>T XP_011515506.1:p.Asn433=
XM_011517206.2:c.1449C>T XP_011515508.1:p.Asn483=
XM_017013716.1:c.1449C>T XP_016869205.1:p.Asn483=
XR_001745568.1:n.1466C>T
XR_001745569.1:n.1466C>T
XR_001745570.1:n.1466C>T
XR_928343.2:n.1466C>T
NM_020863.4:c.1485C>T MANE Select NP_065914.2:p.Asn495=
NM_001029939.4:c.1449C>T NP_001025110.2:p.Asn483=
NM_001167583.3:c.1449C>T NP_001161055.1:p.Asn483=
NM_001174157.2:c.1299C>T NP_001167628.1:p.Asn433=
NM_001174158.2:c.1449C>T NP_001167629.1:p.Asn483=
NM_001289394.2:c.1449C>T NP_001276323.1:p.Asn483=
NR_110323.2:n.1653C>T