Canonical Allele Identifier: CA4888229

Gene: ZFAT

Linked Data

• dbSNP Id: rs557015063
• ExAC: 8:135622762 C / T
• gnomAD v2: 8-135622762-C-T
• gnomAD v3: 8-134610519-C-T
• gnomAD v4: 8-134610519-C-T
• MyVariant Identifiers: chr8:g.135622762C>T (hg19) ; chr8:g.134610519C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.134610519C>T , CM000670.2:g.134610519C>T	GRCh38
NC_000008.10:g.135622762C>T , CM000670.1:g.135622762C>T	GRCh37
NC_000008.9:g.135691944C>T	NCBI36
NG_016356.1:g.107531G>A
NG_016356.2:g.107531G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377838.8:c.585G>A MANE Select	ENSP00000367069.3:p.Ala195=
ENST00000377838.7:c.585G>A	ENSP00000367069.3:p.Ala195=
ENST00000429442.6:c.549G>A	ENSP00000394501.2:p.Ala183=
ENST00000518191.1:c.413-1640G>A	ENSP00000428192.1:n.413-1640G>A
ENST00000520214.5:c.549G>A	ENSP00000428483.1:p.Ala183=
ENST00000520356.5:c.549G>A	ENSP00000427879.1:p.Ala183=
ENST00000520727.5:c.549G>A	ENSP00000427831.1:p.Ala183=
ENST00000522257.5:c.399G>A	ENSP00000429983.1:p.Ala133=
ENST00000522974.5:n.690G>A
ENST00000523040.1:n.270G>A
ENST00000523243.5:c.585G>A	ENSP00000429930.1:p.Ala195=
ENST00000523399.5:c.449-1640G>A	ENSP00000429091.1:n.449-1640G>A
ENST00000523924.5:c.*567G>A	ENSP00000429050.1:n.*567G>A
NM_001029939.3:c.549G>A	NP_001025110.2:p.Ala183=
NM_001167583.2:c.549G>A	NP_001161055.1:p.Ala183=
NM_001174157.1:c.449-1640G>A	NP_001167628.1:n.449-1640G>A
NM_001174158.1:c.549G>A	NP_001167629.1:p.Ala183=
NM_001289394.1:c.549G>A	NP_001276323.1:p.Ala183=
NM_020863.3:c.585G>A	NP_065914.2:p.Ala195=
NR_110323.1:n.771G>A
XM_011517203.1:c.549G>A	XP_011515505.1:p.Ala183=
XM_011517204.1:c.399G>A	XP_011515506.1:p.Ala133=
XM_011517205.1:c.549G>A	XP_011515507.1:p.Ala183=
XM_011517206.1:c.549G>A	XP_011515508.1:p.Ala183=
XR_928343.1:n.566G>A
XM_011517204.2:c.399G>A	XP_011515506.1:p.Ala133=
XM_011517206.2:c.549G>A	XP_011515508.1:p.Ala183=
XM_017013716.1:c.549G>A	XP_016869205.1:p.Ala183=
XR_001745568.1:n.566G>A
XR_001745569.1:n.566G>A
XR_001745570.1:n.566G>A
XR_928343.2:n.566G>A
NM_020863.4:c.585G>A MANE Select	NP_065914.2:p.Ala195=
NM_001029939.4:c.549G>A	NP_001025110.2:p.Ala183=
NM_001167583.3:c.549G>A	NP_001161055.1:p.Ala183=
NM_001174157.2:c.449-1640G>A	NP_001167628.1:n.449-1640G>A
NM_001174158.2:c.549G>A	NP_001167629.1:p.Ala183=
NM_001289394.2:c.549G>A	NP_001276323.1:p.Ala183=
NR_110323.2:n.753G>A