Canonical Allele Identifier: CA1821821543

Gene: ZFAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.134602420G= , CM000670.2:g.134602420G=	GRCh38
NC_000008.10:g.135614663G= , CM000670.1:g.135614663G=	GRCh37
NC_000008.9:g.135683845G=	NCBI36
NG_016356.1:g.115630C=
NG_016356.2:g.115630C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377838.8:c.1299C= MANE Select	ENSP00000367069.3:p.Ala433=
ENST00000377838.7:c.1299C=	ENSP00000367069.3:p.Ala433=
ENST00000429442.6:c.1263C=	ENSP00000394501.2:p.Ala421=
ENST00000520214.5:c.1263C=	ENSP00000428483.1:p.Ala421=
ENST00000520356.5:c.1263C=	ENSP00000427879.1:p.Ala421=
ENST00000520727.5:c.1263C=	ENSP00000427831.1:p.Ala421=
ENST00000522974.5:n.1404C=
ENST00000523243.5:c.1299C=	ENSP00000429930.1:p.Ala433=
ENST00000523399.5:c.1113C=	ENSP00000429091.1:p.Ala371=
ENST00000523924.5:c.*1281C=	ENSP00000429050.1:n.*1281C=
NM_001029939.3:c.1263C=	NP_001025110.2:p.Ala421=
NM_001167583.2:c.1263C=	NP_001161055.1:p.Ala421=
NM_001174157.1:c.1113C=	NP_001167628.1:p.Ala371=
NM_001174158.1:c.1263C=	NP_001167629.1:p.Ala421=
NM_001289394.1:c.1263C=	NP_001276323.1:p.Ala421=
NM_020863.3:c.1299C=	NP_065914.2:p.Ala433=
NR_110323.1:n.1485C=
XM_011517203.1:c.1263C=	XP_011515505.1:p.Ala421=
XM_011517204.1:c.1113C=	XP_011515506.1:p.Ala371=
XM_011517205.1:c.1263C=	XP_011515507.1:p.Ala421=
XM_011517206.1:c.1263C=	XP_011515508.1:p.Ala421=
XR_928343.1:n.1280C=
XM_011517204.2:c.1113C=	XP_011515506.1:p.Ala371=
XM_011517206.2:c.1263C=	XP_011515508.1:p.Ala421=
XM_017013716.1:c.1263C=	XP_016869205.1:p.Ala421=
XR_001745568.1:n.1280C=
XR_001745569.1:n.1280C=
XR_001745570.1:n.1280C=
XR_928343.2:n.1280C=
NM_020863.4:c.1299C= MANE Select	NP_065914.2:p.Ala433=
NM_001029939.4:c.1263C=	NP_001025110.2:p.Ala421=
NM_001167583.3:c.1263C=	NP_001161055.1:p.Ala421=
NM_001174157.2:c.1113C=	NP_001167628.1:p.Ala371=
NM_001174158.2:c.1263C=	NP_001167629.1:p.Ala421=
NM_001289394.2:c.1263C=	NP_001276323.1:p.Ala421=
NR_110323.2:n.1467C=