Canonical Allele Identifier: CA347788105

Gene: ZAP70

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97724145C>G , CM000664.2:g.97724145C>G	GRCh38
NC_000002.11:g.98340608C>G , CM000664.1:g.98340608C>G	GRCh37
NC_000002.10:g.97707040C>G	NCBI36
NG_007727.1:g.15578C>G , LRG_126:g.15578C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001079.4:c.109C>G MANE Select	NP_001070.2:p.Arg37Gly
ENST00000264972.10:c.109C>G MANE Select	ENSP00000264972.5:p.Arg37Gly
NM_001079.3:c.109C>G , LRG_126t1:c.109C>G	NP_001070.2:p.Arg37Gly
NM_001378594.1:c.109C>G	NP_001365523.1:p.Arg37Gly
ENST00000264972.9:c.109C>G	ENSP00000264972.5:p.Arg37Gly
ENST00000483781.5:n.302C>G
ENST00000698508.1:c.109C>G	ENSP00000513759.1:p.Arg37Gly
ENST00000698509.1:n.249C>G
XM_005264015.3:c.109C>G	XP_005264072.1:p.Arg37Gly
XM_006712728.2:c.109C>G	XP_006712791.1:p.Arg37Gly
XM_011511783.1:c.109C>G	XP_011510085.1:p.Arg37Gly
XM_017004867.1:c.478C>G	XP_016860356.1:p.Arg160Gly
XM_017004868.1:c.478C>G	XP_016860357.1:p.Arg160Gly
XM_017004869.1:c.478C>G	XP_016860358.1:p.Arg160Gly
XM_017004870.1:c.478C>G	XP_016860359.1:p.Arg160Gly
XR_001738925.1:n.1717C>G
XR_001738926.1:n.1717C>G
XR_001738927.1:n.1717C>G
XR_923018.1:n.311C>G
XR_923019.1:n.311C>G
XR_923020.1:n.311C>G