Canonical Allele Identifier: CA52553241

Gene: ZAP70

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97724228G>C , CM000664.2:g.97724228G>C	GRCh38
NC_000002.11:g.98340691G>C , CM000664.1:g.98340691G>C	GRCh37
NC_000002.10:g.97707123G>C	NCBI36
NG_007727.1:g.15661G>C , LRG_126:g.15661G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.192G>C	ENSP00000513759.1:p.Gln64His
ENST00000698509.1:n.332G>C
ENST00000264972.10:c.192G>C MANE Select	ENSP00000264972.5:p.Gln64His
ENST00000264972.9:c.192G>C	ENSP00000264972.5:p.Gln64His
ENST00000483781.5:n.385G>C
NM_001079.3:c.192G>C , LRG_126t1:c.192G>C	NP_001070.2:p.Gln64His
XM_005264015.3:c.192G>C	XP_005264072.1:p.Gln64His
XM_006712728.2:c.192G>C	XP_006712791.1:p.Gln64His
XM_011511783.1:c.192G>C	XP_011510085.1:p.Gln64His
XR_923018.1:n.394G>C
XR_923019.1:n.394G>C
XR_923020.1:n.394G>C
XM_017004867.1:c.561G>C	XP_016860356.1:p.Gln187His
XM_017004868.1:c.561G>C	XP_016860357.1:p.Gln187His
XM_017004869.1:c.561G>C	XP_016860358.1:p.Gln187His
XM_017004870.1:c.561G>C	XP_016860359.1:p.Gln187His
XR_001738925.1:n.1800G>C
XR_001738926.1:n.1800G>C
XR_001738927.1:n.1800G>C
NM_001079.4:c.192G>C MANE Select	NP_001070.2:p.Gln64His
NM_001378594.1:c.192G>C	NP_001365523.1:p.Gln64His