Canonical Allele Identifier: CA2581808890

Gene: ZAP70

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737384C>G , CM000664.2:g.97737384C>G	GRCh38
NC_000002.11:g.98353847C>G , CM000664.1:g.98353847C>G	GRCh37
NC_000002.10:g.97720279C>G	NCBI36
NG_007727.1:g.28817C>G , LRG_126:g.28817C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1290-89C>G	ENSP00000513759.1:n.1290-89C>G
ENST00000698509.1:n.1430-89C>G
ENST00000264972.10:c.1290-89C>G MANE Select	ENSP00000264972.5:n.1290-89C>G
ENST00000264972.9:c.1290-89C>G	ENSP00000264972.5:n.1290-89C>G
ENST00000451498.2:c.369-89C>G	ENSP00000400475.2:n.369-89C>G
ENST00000463643.5:n.1151-89C>G
ENST00000487283.5:n.2342-89C>G
ENST00000495754.1:n.228-89C>G
NM_001079.3:c.1290-89C>G , LRG_126t1:c.1290-89C>G	NP_001070.2:n.1290-89C>G
NM_207519.1:c.369-89C>G	NP_997402.1:n.369-89C>G
XM_005264015.3:c.1272-89C>G	XP_005264072.1:n.1272-89C>G
XM_006712728.2:c.1290-89C>G	XP_006712791.1:n.1290-89C>G
XM_011511783.1:c.1290-89C>G	XP_011510085.1:n.1290-89C>G
XR_923018.1:n.1492-89C>G
XR_923019.1:n.1492-89C>G
XR_923020.1:n.1492-89C>G
XM_017004867.1:c.1659-89C>G	XP_016860356.1:n.1659-89C>G
XM_017004868.1:c.1641-89C>G	XP_016860357.1:n.1641-89C>G
XM_017004869.1:c.1659-89C>G	XP_016860358.1:n.1659-89C>G
XM_017004870.1:c.1659-89C>G	XP_016860359.1:n.1659-89C>G
XR_001738925.1:n.2898-89C>G
XR_001738926.1:n.2898-89C>G
XR_001738927.1:n.2898-89C>G
NM_001079.4:c.1290-89C>G MANE Select	NP_001070.2:n.1290-89C>G
NM_001378594.1:c.1290-89C>G	NP_001365523.1:n.1290-89C>G
NM_207519.2:c.369-89C>G	NP_997402.1:n.369-89C>G