Canonical Allele Identifier: CA52544997

Gene: ZAP70

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97713816_97713823del , CM000664.2:g.97713816_97713823del	GRCh38
NC_000002.11:g.98330279_98330286del , CM000664.1:g.98330279_98330286del	GRCh37
NC_000002.10:g.97696711_97696718del	NCBI36
NG_007727.1:g.5249_5256del , LRG_126:g.5249_5256del

Transcript Alleles

HGVS	Amino-acid Change
NM_001079.4:c.-100-100_-100-93del MANE Select	NP_001070.2:n.-100-100_-100-93del
ENST00000264972.10:c.-100-100_-100-93del MANE Select	ENSP00000264972.5:n.-100-100_-100-93del
NM_001079.3:c.-100-100_-100-93del , LRG_126t1:c.-100-100_-100-93del	NP_001070.2:n.-100-100_-100-93del
ENST00000264972.9:c.-100-100_-100-93del	ENSP00000264972.5:n.-100-100_-100-93del
ENST00000483781.5:n.94-100_94-93del
ENST00000698508.1:c.-200_-193del	ENSP00000513759.1:n.-200_-193del
XM_005264015.3:c.-100-100_-100-93del	XP_005264072.1:n.-100-100_-100-93del
XM_006712728.2:c.-100-100_-100-93del	XP_006712791.1:n.-100-100_-100-93del
XM_011511783.1:c.-100-100_-100-93del	XP_011510085.1:n.-100-100_-100-93del
XM_017004867.1:c.165-100_165-93del	XP_016860356.1:n.165-100_165-93del
XM_017004868.1:c.165-100_165-93del	XP_016860357.1:n.165-100_165-93del
XM_017004869.1:c.165-100_165-93del	XP_016860358.1:n.165-100_165-93del
XM_017004870.1:c.165-100_165-93del	XP_016860359.1:n.165-100_165-93del
XR_001738925.1:n.1404-100_1404-93del
XR_001738926.1:n.1404-100_1404-93del
XR_001738927.1:n.1404-100_1404-93del
XR_923018.1:n.103-100_103-93del
XR_923019.1:n.103-100_103-93del
XR_923020.1:n.103-100_103-93del