Canonical Allele Identifier: CA372076517

Gene: ZFAT

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.134520989C>G , CM000670.2:g.134520989C>G	GRCh38
NC_000008.10:g.135533232C>G , CM000670.1:g.135533232C>G	GRCh37
NC_000008.9:g.135602414C>G	NCBI36
NG_016356.1:g.197061G>C
NG_016356.2:g.197061G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377838.8:c.3128G>C MANE Select	ENSP00000367069.3:p.Cys1043Ser
ENST00000377838.7:c.3128G>C	ENSP00000367069.3:p.Cys1043Ser
ENST00000429442.6:c.3092G>C	ENSP00000394501.2:p.Cys1031Ser
ENST00000517307.5:n.732G>C
ENST00000518408.5:n.491G>C
ENST00000520214.5:c.3092G>C	ENSP00000428483.1:p.Cys1031Ser
ENST00000520356.5:c.3092G>C	ENSP00000427879.1:p.Cys1031Ser
ENST00000520727.5:c.3092G>C	ENSP00000427831.1:p.Cys1031Ser
ENST00000523243.5:c.*297G>C	ENSP00000429930.1:n.*297G>C
ENST00000523399.5:c.2942G>C	ENSP00000429091.1:p.Cys981Ser
ENST00000523924.5:c.*3110G>C	ENSP00000429050.1:n.*3110G>C
NM_001029939.3:c.3092G>C	NP_001025110.2:p.Cys1031Ser
NM_001167583.2:c.3092G>C	NP_001161055.1:p.Cys1031Ser
NM_001174157.1:c.2942G>C	NP_001167628.1:p.Cys981Ser
NM_001174158.1:c.3092G>C	NP_001167629.1:p.Cys1031Ser
NM_001289394.1:c.3092G>C	NP_001276323.1:p.Cys1031Ser
NM_020863.3:c.3128G>C	NP_065914.2:p.Cys1043Ser
NR_110323.1:n.3480G>C
XM_011517203.1:c.3092G>C	XP_011515505.1:p.Cys1031Ser
XM_011517204.1:c.2942G>C	XP_011515506.1:p.Cys981Ser
XM_011517206.1:c.3092G>C	XP_011515508.1:p.Cys1031Ser
XR_928343.1:n.3109G>C
XM_011517204.2:c.2942G>C	XP_011515506.1:p.Cys981Ser
XM_011517206.2:c.3092G>C	XP_011515508.1:p.Cys1031Ser
XM_017013716.1:c.3092G>C	XP_016869205.1:p.Cys1031Ser
XR_001745569.1:n.3020G>C
XR_928343.2:n.3109G>C
NM_020863.4:c.3128G>C MANE Select	NP_065914.2:p.Cys1043Ser
NM_001029939.4:c.3092G>C	NP_001025110.2:p.Cys1031Ser
NM_001167583.3:c.3092G>C	NP_001161055.1:p.Cys1031Ser
NM_001174157.2:c.2942G>C	NP_001167628.1:p.Cys981Ser
NM_001174158.2:c.3092G>C	NP_001167629.1:p.Cys1031Ser
NM_001289394.2:c.3092G>C	NP_001276323.1:p.Cys1031Ser
NR_110323.2:n.3462G>C