Canonical Allele Identifier: CA1273122329

Gene: ZAP70

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737508T= , CM000664.2:g.97737508T=	GRCh38
NC_000002.11:g.98353971T= , CM000664.1:g.98353971T=	GRCh37
NC_000002.10:g.97720403T=	NCBI36
NG_007727.1:g.28941T= , LRG_126:g.28941T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1325T=	ENSP00000513759.1:p.Leu442=
ENST00000698509.1:n.1465T=
ENST00000264972.10:c.1325T= MANE Select	ENSP00000264972.5:p.Leu442=
ENST00000264972.9:c.1325T=	ENSP00000264972.5:p.Leu442=
ENST00000451498.2:c.404T=	ENSP00000400475.2:p.Leu135=
ENST00000463643.5:n.1186T=
ENST00000487283.5:n.2377T=
ENST00000495754.1:n.263T=
NM_001079.3:c.1325T= , LRG_126t1:c.1325T=	NP_001070.2:p.Leu442=
NM_207519.1:c.404T=	NP_997402.1:p.Leu135=
XM_005264015.3:c.1307T=	XP_005264072.1:p.Leu436=
XM_006712728.2:c.1325T=	XP_006712791.1:p.Leu442=
XM_011511783.1:c.1325T=	XP_011510085.1:p.Leu442=
XR_923018.1:n.1527T=
XR_923019.1:n.1527T=
XR_923020.1:n.1527T=
XM_017004867.1:c.1694T=	XP_016860356.1:p.Leu565=
XM_017004868.1:c.1676T=	XP_016860357.1:p.Leu559=
XM_017004869.1:c.1694T=	XP_016860358.1:p.Leu565=
XM_017004870.1:c.1694T=	XP_016860359.1:p.Leu565=
XR_001738925.1:n.2933T=
XR_001738926.1:n.2933T=
XR_001738927.1:n.2933T=
NM_001079.4:c.1325T= MANE Select	NP_001070.2:p.Leu442=
NM_001378594.1:c.1325T=	NP_001365523.1:p.Leu442=
NM_207519.2:c.404T=	NP_997402.1:p.Leu135=