Canonical Allele Identifier: CA186422407

Gene: ZFAT

Linked Data

• dbSNP Id: rs973225109
• MyVariant Identifiers: chr8:g.135636808G>C (hg19) ; chr8:g.134624565G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.134624565G>C , CM000670.2:g.134624565G>C	GRCh38
NC_000008.10:g.135636808G>C , CM000670.1:g.135636808G>C	GRCh37
NC_000008.9:g.135705990G>C	NCBI36
NG_016356.1:g.93485C>G
NG_016356.2:g.93485C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377838.8:c.448+12896C>G MANE Select	ENSP00000367069.3:n.448+12896C>G
ENST00000377838.7:c.448+12896C>G	ENSP00000367069.3:n.448+12896C>G
ENST00000429442.6:c.412+12896C>G	ENSP00000394501.2:n.412+12896C>G
ENST00000518191.1:c.412+12896C>G	ENSP00000428192.1:n.412+12896C>G
ENST00000520214.5:c.412+12896C>G	ENSP00000428483.1:n.412+12896C>G
ENST00000520356.5:c.412+12896C>G	ENSP00000427879.1:n.412+12896C>G
ENST00000520727.5:c.412+12896C>G	ENSP00000427831.1:n.412+12896C>G
ENST00000522257.5:c.262+12896C>G	ENSP00000429983.1:n.262+12896C>G
ENST00000522974.5:n.553+12896C>G
ENST00000523040.1:n.133+12896C>G
ENST00000523243.5:c.448+12896C>G	ENSP00000429930.1:n.448+12896C>G
ENST00000523399.5:c.448+12896C>G	ENSP00000429091.1:n.448+12896C>G
ENST00000523924.5:c.*430+12896C>G	ENSP00000429050.1:n.*430+12896C>G
NM_001029939.3:c.412+12896C>G	NP_001025110.2:n.412+12896C>G
NM_001167583.2:c.412+12896C>G	NP_001161055.1:n.412+12896C>G
NM_001174157.1:c.448+12896C>G	NP_001167628.1:n.448+12896C>G
NM_001174158.1:c.412+12896C>G	NP_001167629.1:n.412+12896C>G
NM_001289394.1:c.412+12896C>G	NP_001276323.1:n.412+12896C>G
NM_020863.3:c.448+12896C>G	NP_065914.2:n.448+12896C>G
NR_110323.1:n.634+12896C>G
XM_011517203.1:c.412+12896C>G	XP_011515505.1:n.412+12896C>G
XM_011517204.1:c.262+12896C>G	XP_011515506.1:n.262+12896C>G
XM_011517205.1:c.412+12896C>G	XP_011515507.1:n.412+12896C>G
XM_011517206.1:c.412+12896C>G	XP_011515508.1:n.412+12896C>G
XR_928343.1:n.429+12896C>G
XM_011517204.2:c.262+12896C>G	XP_011515506.1:n.262+12896C>G
XM_011517206.2:c.412+12896C>G	XP_011515508.1:n.412+12896C>G
XM_017013716.1:c.412+12896C>G	XP_016869205.1:n.412+12896C>G
XR_001745568.1:n.429+12896C>G
XR_001745569.1:n.429+12896C>G
XR_001745570.1:n.429+12896C>G
XR_928343.2:n.429+12896C>G
NM_020863.4:c.448+12896C>G MANE Select	NP_065914.2:n.448+12896C>G
NM_001029939.4:c.412+12896C>G	NP_001025110.2:n.412+12896C>G
NM_001167583.3:c.412+12896C>G	NP_001161055.1:n.412+12896C>G
NM_001174157.2:c.448+12896C>G	NP_001167628.1:n.448+12896C>G
NM_001174158.2:c.412+12896C>G	NP_001167629.1:n.412+12896C>G
NM_001289394.2:c.412+12896C>G	NP_001276323.1:n.412+12896C>G
NR_110323.2:n.616+12896C>G