Canonical Allele Identifier: CA4888094

Gene: ZFAT

Linked Data

• dbSNP Id: rs375484784
• ExAC: 8:135614837 G / A
• gnomAD v2: 8-135614837-G-A
• gnomAD v4: 8-134602594-G-A
• MyVariant Identifiers: chr8:g.135614837G>A (hg19) ; chr8:g.134602594G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.134602594G>A , CM000670.2:g.134602594G>A	GRCh38
NC_000008.10:g.135614837G>A , CM000670.1:g.135614837G>A	GRCh37
NC_000008.9:g.135684019G>A	NCBI36
NG_016356.1:g.115456C>T
NG_016356.2:g.115456C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377838.8:c.1125C>T MANE Select	ENSP00000367069.3:p.Asp375=
ENST00000377838.7:c.1125C>T	ENSP00000367069.3:p.Asp375=
ENST00000429442.6:c.1089C>T	ENSP00000394501.2:p.Asp363=
ENST00000520214.5:c.1089C>T	ENSP00000428483.1:p.Asp363=
ENST00000520356.5:c.1089C>T	ENSP00000427879.1:p.Asp363=
ENST00000520727.5:c.1089C>T	ENSP00000427831.1:p.Asp363=
ENST00000522974.5:n.1230C>T
ENST00000523243.5:c.1125C>T	ENSP00000429930.1:p.Asp375=
ENST00000523399.5:c.939C>T	ENSP00000429091.1:p.Asp313=
ENST00000523924.5:c.*1107C>T	ENSP00000429050.1:n.*1107C>T
NM_001029939.3:c.1089C>T	NP_001025110.2:p.Asp363=
NM_001167583.2:c.1089C>T	NP_001161055.1:p.Asp363=
NM_001174157.1:c.939C>T	NP_001167628.1:p.Asp313=
NM_001174158.1:c.1089C>T	NP_001167629.1:p.Asp363=
NM_001289394.1:c.1089C>T	NP_001276323.1:p.Asp363=
NM_020863.3:c.1125C>T	NP_065914.2:p.Asp375=
NR_110323.1:n.1311C>T
XM_011517203.1:c.1089C>T	XP_011515505.1:p.Asp363=
XM_011517204.1:c.939C>T	XP_011515506.1:p.Asp313=
XM_011517205.1:c.1089C>T	XP_011515507.1:p.Asp363=
XM_011517206.1:c.1089C>T	XP_011515508.1:p.Asp363=
XR_928343.1:n.1106C>T
XM_011517204.2:c.939C>T	XP_011515506.1:p.Asp313=
XM_011517206.2:c.1089C>T	XP_011515508.1:p.Asp363=
XM_017013716.1:c.1089C>T	XP_016869205.1:p.Asp363=
XR_001745568.1:n.1106C>T
XR_001745569.1:n.1106C>T
XR_001745570.1:n.1106C>T
XR_928343.2:n.1106C>T
NM_020863.4:c.1125C>T MANE Select	NP_065914.2:p.Asp375=
NM_001029939.4:c.1089C>T	NP_001025110.2:p.Asp363=
NM_001167583.3:c.1089C>T	NP_001161055.1:p.Asp363=
NM_001174157.2:c.939C>T	NP_001167628.1:p.Asp313=
NM_001174158.2:c.1089C>T	NP_001167629.1:p.Asp363=
NM_001289394.2:c.1089C>T	NP_001276323.1:p.Asp363=
NR_110323.2:n.1293C>T