Canonical Allele Identifier: CA186406917

Gene: ZFAT

Linked Data

• dbSNP Id: rs34615535
• MyVariant Identifiers: chr8:g.135614719_135614720insA (hg19) ; chr8:g.134602476_134602477insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.134602476_134602477insA , CM000670.2:g.134602476_134602477insA	GRCh38
NC_000008.10:g.135614719_135614720insA , CM000670.1:g.135614719_135614720insA	GRCh37
NC_000008.9:g.135683901_135683902insA	NCBI36
NG_016356.1:g.115573_115574insT
NG_016356.2:g.115573_115574insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377838.8:c.1242_1243insT MANE Select	ENSP00000367069.3:p.Asn415Ter
ENST00000377838.7:c.1242_1243insT	ENSP00000367069.3:p.Asn415Ter
ENST00000429442.6:c.1206_1207insT	ENSP00000394501.2:p.Asn403Ter
ENST00000520214.5:c.1206_1207insT	ENSP00000428483.1:p.Asn403Ter
ENST00000520356.5:c.1206_1207insT	ENSP00000427879.1:p.Asn403Ter
ENST00000520727.5:c.1206_1207insT	ENSP00000427831.1:p.Asn403Ter
ENST00000522974.5:n.1347_1348insT
ENST00000523243.5:c.1242_1243insT	ENSP00000429930.1:p.Asn415Ter
ENST00000523399.5:c.1056_1057insT	ENSP00000429091.1:p.Asn353Ter
ENST00000523924.5:c.*1224_*1225insT	ENSP00000429050.1:n.*1224_*1225insT
NM_001029939.3:c.1206_1207insT	NP_001025110.2:p.Asn403Ter
NM_001167583.2:c.1206_1207insT	NP_001161055.1:p.Asn403Ter
NM_001174157.1:c.1056_1057insT	NP_001167628.1:p.Asn353Ter
NM_001174158.1:c.1206_1207insT	NP_001167629.1:p.Asn403Ter
NM_001289394.1:c.1206_1207insT	NP_001276323.1:p.Asn403Ter
NM_020863.3:c.1242_1243insT	NP_065914.2:p.Asn415Ter
NR_110323.1:n.1428_1429insT
XM_011517203.1:c.1206_1207insT	XP_011515505.1:p.Asn403Ter
XM_011517204.1:c.1056_1057insT	XP_011515506.1:p.Asn353Ter
XM_011517205.1:c.1206_1207insT	XP_011515507.1:p.Asn403Ter
XM_011517206.1:c.1206_1207insT	XP_011515508.1:p.Asn403Ter
XR_928343.1:n.1223_1224insT
XM_011517204.2:c.1056_1057insT	XP_011515506.1:p.Asn353Ter
XM_011517206.2:c.1206_1207insT	XP_011515508.1:p.Asn403Ter
XM_017013716.1:c.1206_1207insT	XP_016869205.1:p.Asn403Ter
XR_001745568.1:n.1223_1224insT
XR_001745569.1:n.1223_1224insT
XR_001745570.1:n.1223_1224insT
XR_928343.2:n.1223_1224insT
NM_020863.4:c.1242_1243insT MANE Select	NP_065914.2:p.Asn415Ter
NM_001029939.4:c.1206_1207insT	NP_001025110.2:p.Asn403Ter
NM_001167583.3:c.1206_1207insT	NP_001161055.1:p.Asn403Ter
NM_001174157.2:c.1056_1057insT	NP_001167628.1:p.Asn353Ter
NM_001174158.2:c.1206_1207insT	NP_001167629.1:p.Asn403Ter
NM_001289394.2:c.1206_1207insT	NP_001276323.1:p.Asn403Ter
NR_110323.2:n.1410_1411insT