Canonical Allele Identifier: CA1273122351

Gene: ZAP70

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737577G= , CM000664.2:g.97737577G=	GRCh38
NC_000002.11:g.98354040G= , CM000664.1:g.98354040G=	GRCh37
NC_000002.10:g.97720472G=	NCBI36
NG_007727.1:g.29010G= , LRG_126:g.29010G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1394G=	ENSP00000513759.1:p.Arg465=
ENST00000698509.1:n.1534G=
ENST00000264972.10:c.1394G= MANE Select	ENSP00000264972.5:p.Arg465=
ENST00000264972.9:c.1394G=	ENSP00000264972.5:p.Arg465=
ENST00000451498.2:c.473G=	ENSP00000400475.2:p.Arg158=
ENST00000463643.5:n.1255G=
ENST00000487283.5:n.2446G=
ENST00000495754.1:n.332G=
NM_001079.3:c.1394G= , LRG_126t1:c.1394G=	NP_001070.2:p.Arg465=
NM_207519.1:c.473G=	NP_997402.1:p.Arg158=
XM_005264015.3:c.1376G=	XP_005264072.1:p.Arg459=
XM_006712728.2:c.1394G=	XP_006712791.1:p.Arg465=
XM_011511783.1:c.1394G=	XP_011510085.1:p.Arg465=
XR_923018.1:n.1596G=
XR_923019.1:n.1596G=
XR_923020.1:n.1596G=
XM_017004867.1:c.1763G=	XP_016860356.1:p.Arg588=
XM_017004868.1:c.1745G=	XP_016860357.1:p.Arg582=
XM_017004869.1:c.1763G=	XP_016860358.1:p.Arg588=
XM_017004870.1:c.1763G=	XP_016860359.1:p.Arg588=
XR_001738925.1:n.3002G=
XR_001738926.1:n.3002G=
XR_001738927.1:n.3002G=
NM_001079.4:c.1394G= MANE Select	NP_001070.2:p.Arg465=
NM_001378594.1:c.1394G=	NP_001365523.1:p.Arg465=
NM_207519.2:c.473G=	NP_997402.1:p.Arg158=