Canonical Allele Identifier: CA1790463

Gene: ZAP70

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737650C>T , CM000664.2:g.97737650C>T	GRCh38
NC_000002.11:g.98354113C>T , CM000664.1:g.98354113C>T	GRCh37
NC_000002.10:g.97720545C>T	NCBI36
NG_007727.1:g.29083C>T , LRG_126:g.29083C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1467C>T	ENSP00000513759.1:p.Asp489=
ENST00000698509.1:n.1607C>T
ENST00000264972.10:c.1467C>T MANE Select	ENSP00000264972.5:p.Asp489=
ENST00000264972.9:c.1467C>T	ENSP00000264972.5:p.Asp489=
ENST00000451498.2:c.546C>T	ENSP00000400475.2:p.Asp182=
ENST00000463643.5:n.1328C>T
ENST00000487283.5:n.2519C>T
ENST00000495754.1:n.405C>T
NM_001079.3:c.1467C>T , LRG_126t1:c.1467C>T	NP_001070.2:p.Asp489=
NM_207519.1:c.546C>T	NP_997402.1:p.Asp182=
XM_005264015.3:c.1449C>T	XP_005264072.1:p.Asp483=
XM_006712728.2:c.1467C>T	XP_006712791.1:p.Asp489=
XM_011511783.1:c.1467C>T	XP_011510085.1:p.Asp489=
XR_923018.1:n.1669C>T
XR_923019.1:n.1669C>T
XR_923020.1:n.1669C>T
XM_017004867.1:c.1836C>T	XP_016860356.1:p.Asp612=
XM_017004868.1:c.1818C>T	XP_016860357.1:p.Asp606=
XM_017004869.1:c.1836C>T	XP_016860358.1:p.Asp612=
XM_017004870.1:c.1836C>T	XP_016860359.1:p.Asp612=
XR_001738925.1:n.3075C>T
XR_001738926.1:n.3075C>T
XR_001738927.1:n.3075C>T
NM_001079.4:c.1467C>T MANE Select	NP_001070.2:p.Asp489=
NM_001378594.1:c.1467C>T	NP_001365523.1:p.Asp489=
NM_207519.2:c.546C>T	NP_997402.1:p.Asp182=