Canonical Allele Identifier: CA463219656

Gene: ZFAT

Linked Data

• dbSNP Id: rs749287442
• gnomAD v2: 8-135614834-C-A
• gnomAD v4: 8-134602591-C-A
• MyVariant Identifiers: chr8:g.135614834C>A (hg19) ; chr8:g.134602591C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.134602591C>A , CM000670.2:g.134602591C>A	GRCh38
NC_000008.10:g.135614834C>A , CM000670.1:g.135614834C>A	GRCh37
NC_000008.9:g.135684016C>A	NCBI36
NG_016356.1:g.115459G>T
NG_016356.2:g.115459G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377838.8:c.1128G>T MANE Select	ENSP00000367069.3:p.Ala376=
ENST00000377838.7:c.1128G>T	ENSP00000367069.3:p.Ala376=
ENST00000429442.6:c.1092G>T	ENSP00000394501.2:p.Ala364=
ENST00000520214.5:c.1092G>T	ENSP00000428483.1:p.Ala364=
ENST00000520356.5:c.1092G>T	ENSP00000427879.1:p.Ala364=
ENST00000520727.5:c.1092G>T	ENSP00000427831.1:p.Ala364=
ENST00000522974.5:n.1233G>T
ENST00000523243.5:c.1128G>T	ENSP00000429930.1:p.Ala376=
ENST00000523399.5:c.942G>T	ENSP00000429091.1:p.Ala314=
ENST00000523924.5:c.*1110G>T	ENSP00000429050.1:n.*1110G>T
NM_001029939.3:c.1092G>T	NP_001025110.2:p.Ala364=
NM_001167583.2:c.1092G>T	NP_001161055.1:p.Ala364=
NM_001174157.1:c.942G>T	NP_001167628.1:p.Ala314=
NM_001174158.1:c.1092G>T	NP_001167629.1:p.Ala364=
NM_001289394.1:c.1092G>T	NP_001276323.1:p.Ala364=
NM_020863.3:c.1128G>T	NP_065914.2:p.Ala376=
NR_110323.1:n.1314G>T
XM_011517203.1:c.1092G>T	XP_011515505.1:p.Ala364=
XM_011517204.1:c.942G>T	XP_011515506.1:p.Ala314=
XM_011517205.1:c.1092G>T	XP_011515507.1:p.Ala364=
XM_011517206.1:c.1092G>T	XP_011515508.1:p.Ala364=
XR_928343.1:n.1109G>T
XM_011517204.2:c.942G>T	XP_011515506.1:p.Ala314=
XM_011517206.2:c.1092G>T	XP_011515508.1:p.Ala364=
XM_017013716.1:c.1092G>T	XP_016869205.1:p.Ala364=
XR_001745568.1:n.1109G>T
XR_001745569.1:n.1109G>T
XR_001745570.1:n.1109G>T
XR_928343.2:n.1109G>T
NM_020863.4:c.1128G>T MANE Select	NP_065914.2:p.Ala376=
NM_001029939.4:c.1092G>T	NP_001025110.2:p.Ala364=
NM_001167583.3:c.1092G>T	NP_001161055.1:p.Ala364=
NM_001174157.2:c.942G>T	NP_001167628.1:p.Ala314=
NM_001174158.2:c.1092G>T	NP_001167629.1:p.Ala364=
NM_001289394.2:c.1092G>T	NP_001276323.1:p.Ala364=
NR_110323.2:n.1296G>T