Canonical Allele Identifier: CA1273122372

Gene: ZAP70

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737623T= , CM000664.2:g.97737623T=	GRCh38
NC_000002.11:g.98354086T= , CM000664.1:g.98354086T=	GRCh37
NC_000002.10:g.97720518T=	NCBI36
NG_007727.1:g.29056T= , LRG_126:g.29056T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1440T=	ENSP00000513759.1:p.Phe480=
ENST00000698509.1:n.1580T=
ENST00000264972.10:c.1440T= MANE Select	ENSP00000264972.5:p.Phe480=
ENST00000264972.9:c.1440T=	ENSP00000264972.5:p.Phe480=
ENST00000451498.2:c.519T=	ENSP00000400475.2:p.Phe173=
ENST00000463643.5:n.1301T=
ENST00000487283.5:n.2492T=
ENST00000495754.1:n.378T=
NM_001079.3:c.1440T= , LRG_126t1:c.1440T=	NP_001070.2:p.Phe480=
NM_207519.1:c.519T=	NP_997402.1:p.Phe173=
XM_005264015.3:c.1422T=	XP_005264072.1:p.Phe474=
XM_006712728.2:c.1440T=	XP_006712791.1:p.Phe480=
XM_011511783.1:c.1440T=	XP_011510085.1:p.Phe480=
XR_923018.1:n.1642T=
XR_923019.1:n.1642T=
XR_923020.1:n.1642T=
XM_017004867.1:c.1809T=	XP_016860356.1:p.Phe603=
XM_017004868.1:c.1791T=	XP_016860357.1:p.Phe597=
XM_017004869.1:c.1809T=	XP_016860358.1:p.Phe603=
XM_017004870.1:c.1809T=	XP_016860359.1:p.Phe603=
XR_001738925.1:n.3048T=
XR_001738926.1:n.3048T=
XR_001738927.1:n.3048T=
NM_001079.4:c.1440T= MANE Select	NP_001070.2:p.Phe480=
NM_001378594.1:c.1440T=	NP_001365523.1:p.Phe480=
NM_207519.2:c.519T=	NP_997402.1:p.Phe173=