Canonical Allele Identifier: CA895855129

Gene: ZAP70

Linked Data

• dbSNP Id: rs1415849817
• MyVariant Identifiers: chr2:g.98354002_98354004del (hg19) ; chr2:g.97737539_97737541del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737543_97737545del , CM000664.2:g.97737543_97737545del	GRCh38
NC_000002.11:g.98354006_98354008del , CM000664.1:g.98354006_98354008del	GRCh37
NC_000002.10:g.97720438_97720440del	NCBI36
NG_007727.1:g.28976_28978del , LRG_126:g.28976_28978del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1360_1362del	ENSP00000513759.1:p.Glu454del
ENST00000698509.1:n.1500_1502del
ENST00000264972.10:c.1360_1362del MANE Select	ENSP00000264972.5:p.Glu454del
ENST00000264972.9:c.1360_1362del	ENSP00000264972.5:p.Glu454del
ENST00000451498.2:c.439_441del	ENSP00000400475.2:p.Glu147del
ENST00000463643.5:n.1221_1223del
ENST00000487283.5:n.2412_2414del
ENST00000495754.1:n.298_300del
NM_001079.3:c.1360_1362del , LRG_126t1:c.1360_1362del	NP_001070.2:p.Glu454del
NM_207519.1:c.439_441del	NP_997402.1:p.Glu147del
XM_005264015.3:c.1342_1344del	XP_005264072.1:p.Glu448del
XM_006712728.2:c.1360_1362del	XP_006712791.1:p.Glu454del
XM_011511783.1:c.1360_1362del	XP_011510085.1:p.Glu454del
XR_923018.1:n.1562_1564del
XR_923019.1:n.1562_1564del
XR_923020.1:n.1562_1564del
XM_017004867.1:c.1729_1731del	XP_016860356.1:p.Glu577del
XM_017004868.1:c.1711_1713del	XP_016860357.1:p.Glu571del
XM_017004869.1:c.1729_1731del	XP_016860358.1:p.Glu577del
XM_017004870.1:c.1729_1731del	XP_016860359.1:p.Glu577del
XR_001738925.1:n.2968_2970del
XR_001738926.1:n.2968_2970del
XR_001738927.1:n.2968_2970del
NM_001079.4:c.1360_1362del MANE Select	NP_001070.2:p.Glu454del
NM_001378594.1:c.1360_1362del	NP_001365523.1:p.Glu454del
NM_207519.2:c.439_441del	NP_997402.1:p.Glu147del