Canonical Allele Identifier: CA372082022

Gene: ZFAT

Linked Data

• MyVariant Identifiers: chr8:g.135622857C>G (hg19) ; chr8:g.134610614C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.134610614C>G , CM000670.2:g.134610614C>G	GRCh38
NC_000008.10:g.135622857C>G , CM000670.1:g.135622857C>G	GRCh37
NC_000008.9:g.135692039C>G	NCBI36
NG_016356.1:g.107436G>C
NG_016356.2:g.107436G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000377838.8:c.490G>C MANE Select	ENSP00000367069.3:p.Asp164His
ENST00000377838.7:c.490G>C	ENSP00000367069.3:p.Asp164His
ENST00000429442.6:c.454G>C	ENSP00000394501.2:p.Asp152His
ENST00000518191.1:c.413-1735G>C	ENSP00000428192.1:n.413-1735G>C
ENST00000520214.5:c.454G>C	ENSP00000428483.1:p.Asp152His
ENST00000520356.5:c.454G>C	ENSP00000427879.1:p.Asp152His
ENST00000520727.5:c.454G>C	ENSP00000427831.1:p.Asp152His
ENST00000522257.5:c.304G>C	ENSP00000429983.1:p.Asp102His
ENST00000522974.5:n.595G>C
ENST00000523040.1:n.175G>C
ENST00000523243.5:c.490G>C	ENSP00000429930.1:p.Asp164His
ENST00000523399.5:c.449-1735G>C	ENSP00000429091.1:n.449-1735G>C
ENST00000523924.5:c.*472G>C	ENSP00000429050.1:n.*472G>C
NM_001029939.3:c.454G>C	NP_001025110.2:p.Asp152His
NM_001167583.2:c.454G>C	NP_001161055.1:p.Asp152His
NM_001174157.1:c.449-1735G>C	NP_001167628.1:n.449-1735G>C
NM_001174158.1:c.454G>C	NP_001167629.1:p.Asp152His
NM_001289394.1:c.454G>C	NP_001276323.1:p.Asp152His
NM_020863.3:c.490G>C	NP_065914.2:p.Asp164His
NR_110323.1:n.676G>C
XM_011517203.1:c.454G>C	XP_011515505.1:p.Asp152His
XM_011517204.1:c.304G>C	XP_011515506.1:p.Asp102His
XM_011517205.1:c.454G>C	XP_011515507.1:p.Asp152His
XM_011517206.1:c.454G>C	XP_011515508.1:p.Asp152His
XR_928343.1:n.471G>C
XM_011517204.2:c.304G>C	XP_011515506.1:p.Asp102His
XM_011517206.2:c.454G>C	XP_011515508.1:p.Asp152His
XM_017013716.1:c.454G>C	XP_016869205.1:p.Asp152His
XR_001745568.1:n.471G>C
XR_001745569.1:n.471G>C
XR_001745570.1:n.471G>C
XR_928343.2:n.471G>C
NM_020863.4:c.490G>C MANE Select	NP_065914.2:p.Asp164His
NM_001029939.4:c.454G>C	NP_001025110.2:p.Asp152His
NM_001167583.3:c.454G>C	NP_001161055.1:p.Asp152His
NM_001174157.2:c.449-1735G>C	NP_001167628.1:n.449-1735G>C
NM_001174158.2:c.454G>C	NP_001167629.1:p.Asp152His
NM_001289394.2:c.454G>C	NP_001276323.1:p.Asp152His
NR_110323.2:n.658G>C