Canonical Allele Identifier: CA1790018

Gene: ZAP70

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97724141G>A , CM000664.2:g.97724141G>A	GRCh38
NC_000002.11:g.98340604G>A , CM000664.1:g.98340604G>A	GRCh37
NC_000002.10:g.97707036G>A	NCBI36
NG_007727.1:g.15574G>A , LRG_126:g.15574G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.105G>A	ENSP00000513759.1:p.Leu35=
ENST00000698509.1:n.245G>A
ENST00000264972.10:c.105G>A MANE Select	ENSP00000264972.5:p.Leu35=
ENST00000264972.9:c.105G>A	ENSP00000264972.5:p.Leu35=
ENST00000483781.5:n.298G>A
NM_001079.3:c.105G>A , LRG_126t1:c.105G>A	NP_001070.2:p.Leu35=
XM_005264015.3:c.105G>A	XP_005264072.1:p.Leu35=
XM_006712728.2:c.105G>A	XP_006712791.1:p.Leu35=
XM_011511783.1:c.105G>A	XP_011510085.1:p.Leu35=
XR_923018.1:n.307G>A
XR_923019.1:n.307G>A
XR_923020.1:n.307G>A
XM_017004867.1:c.474G>A	XP_016860356.1:p.Leu158=
XM_017004868.1:c.474G>A	XP_016860357.1:p.Leu158=
XM_017004869.1:c.474G>A	XP_016860358.1:p.Leu158=
XM_017004870.1:c.474G>A	XP_016860359.1:p.Leu158=
XR_001738925.1:n.1713G>A
XR_001738926.1:n.1713G>A
XR_001738927.1:n.1713G>A
NM_001079.4:c.105G>A MANE Select	NP_001070.2:p.Leu35=
NM_001378594.1:c.105G>A	NP_001365523.1:p.Leu35=