Canonical Allele Identifier: CA463219392

Gene: ZFAT

Linked Data

• MyVariant Identifiers: chr8:g.135614762C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.134602519C>G , CM000670.2:g.134602519C>G	GRCh38
NC_000008.10:g.135614762C>G , CM000670.1:g.135614762C>G	GRCh37
NC_000008.9:g.135683944C>G	NCBI36
NG_016356.1:g.115531G>C
NG_016356.2:g.115531G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377838.8:c.1200G>C MANE Select	ENSP00000367069.3:p.Arg400=
ENST00000377838.7:c.1200G>C	ENSP00000367069.3:p.Arg400=
ENST00000429442.6:c.1164G>C	ENSP00000394501.2:p.Arg388=
ENST00000520214.5:c.1164G>C	ENSP00000428483.1:p.Arg388=
ENST00000520356.5:c.1164G>C	ENSP00000427879.1:p.Arg388=
ENST00000520727.5:c.1164G>C	ENSP00000427831.1:p.Arg388=
ENST00000522974.5:n.1305G>C
ENST00000523243.5:c.1200G>C	ENSP00000429930.1:p.Arg400=
ENST00000523399.5:c.1014G>C	ENSP00000429091.1:p.Arg338=
ENST00000523924.5:c.*1182G>C	ENSP00000429050.1:n.*1182G>C
NM_001029939.3:c.1164G>C	NP_001025110.2:p.Arg388=
NM_001167583.2:c.1164G>C	NP_001161055.1:p.Arg388=
NM_001174157.1:c.1014G>C	NP_001167628.1:p.Arg338=
NM_001174158.1:c.1164G>C	NP_001167629.1:p.Arg388=
NM_001289394.1:c.1164G>C	NP_001276323.1:p.Arg388=
NM_020863.3:c.1200G>C	NP_065914.2:p.Arg400=
NR_110323.1:n.1386G>C
XM_011517203.1:c.1164G>C	XP_011515505.1:p.Arg388=
XM_011517204.1:c.1014G>C	XP_011515506.1:p.Arg338=
XM_011517205.1:c.1164G>C	XP_011515507.1:p.Arg388=
XM_011517206.1:c.1164G>C	XP_011515508.1:p.Arg388=
XR_928343.1:n.1181G>C
XM_011517204.2:c.1014G>C	XP_011515506.1:p.Arg338=
XM_011517206.2:c.1164G>C	XP_011515508.1:p.Arg388=
XM_017013716.1:c.1164G>C	XP_016869205.1:p.Arg388=
XR_001745568.1:n.1181G>C
XR_001745569.1:n.1181G>C
XR_001745570.1:n.1181G>C
XR_928343.2:n.1181G>C
NM_020863.4:c.1200G>C MANE Select	NP_065914.2:p.Arg400=
NM_001029939.4:c.1164G>C	NP_001025110.2:p.Arg388=
NM_001167583.3:c.1164G>C	NP_001161055.1:p.Arg388=
NM_001174157.2:c.1014G>C	NP_001167628.1:p.Arg338=
NM_001174158.2:c.1164G>C	NP_001167629.1:p.Arg388=
NM_001289394.2:c.1164G>C	NP_001276323.1:p.Arg388=
NR_110323.2:n.1368G>C