Canonical Allele Identifier: CA4887561

Gene: ZFAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.134532867C>T , CM000670.2:g.134532867C>T	GRCh38
NC_000008.10:g.135545110C>T , CM000670.1:g.135545110C>T	GRCh37
NC_000008.9:g.135614292C>T	NCBI36
NG_016356.1:g.185183G>A
NG_016356.2:g.185183G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377838.8:c.3082G>A MANE Select	ENSP00000367069.3:p.Gly1028Arg
ENST00000377838.7:c.3082G>A	ENSP00000367069.3:p.Gly1028Arg
ENST00000429442.6:c.3046G>A	ENSP00000394501.2:p.Gly1016Arg
ENST00000517307.5:n.686G>A
ENST00000518408.5:n.445G>A
ENST00000520214.5:c.3046G>A	ENSP00000428483.1:p.Gly1016Arg
ENST00000520356.5:c.3046G>A	ENSP00000427879.1:p.Gly1016Arg
ENST00000520727.5:c.3046G>A	ENSP00000427831.1:p.Gly1016Arg
ENST00000523243.5:c.*251G>A	ENSP00000429930.1:n.*251G>A
ENST00000523399.5:c.2896G>A	ENSP00000429091.1:p.Gly966Arg
ENST00000523924.5:c.*3064G>A	ENSP00000429050.1:n.*3064G>A
NM_001029939.3:c.3046G>A	NP_001025110.2:p.Gly1016Arg
NM_001167583.2:c.3046G>A	NP_001161055.1:p.Gly1016Arg
NM_001174157.1:c.2896G>A	NP_001167628.1:p.Gly966Arg
NM_001174158.1:c.3046G>A	NP_001167629.1:p.Gly1016Arg
NM_001289394.1:c.3046G>A	NP_001276323.1:p.Gly1016Arg
NM_020863.3:c.3082G>A	NP_065914.2:p.Gly1028Arg
NR_110323.1:n.3434G>A
XM_011517203.1:c.3046G>A	XP_011515505.1:p.Gly1016Arg
XM_011517204.1:c.2896G>A	XP_011515506.1:p.Gly966Arg
XM_011517206.1:c.3046G>A	XP_011515508.1:p.Gly1016Arg
XR_928343.1:n.3063G>A
XM_011517204.2:c.2896G>A	XP_011515506.1:p.Gly966Arg
XM_011517206.2:c.3046G>A	XP_011515508.1:p.Gly1016Arg
XM_017013716.1:c.3046G>A	XP_016869205.1:p.Gly1016Arg
XR_001745569.1:n.2974G>A
XR_928343.2:n.3063G>A
NM_020863.4:c.3082G>A MANE Select	NP_065914.2:p.Gly1028Arg
NM_001029939.4:c.3046G>A	NP_001025110.2:p.Gly1016Arg
NM_001167583.3:c.3046G>A	NP_001161055.1:p.Gly1016Arg
NM_001174157.2:c.2896G>A	NP_001167628.1:p.Gly966Arg
NM_001174158.2:c.3046G>A	NP_001167629.1:p.Gly1016Arg
NM_001289394.2:c.3046G>A	NP_001276323.1:p.Gly1016Arg
NR_110323.2:n.3416G>A