Canonical Allele Identifier: CA2660262519

Gene: ZAP70

Linked Data

• gnomAD v4: 2-97737420-TGGGAACTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737422_97737430del , CM000664.2:g.97737422_97737430del	GRCh38
NC_000002.11:g.98353885_98353893del , CM000664.1:g.98353885_98353893del	GRCh37
NC_000002.10:g.97720317_97720325del	NCBI36
NG_007727.1:g.28855_28863del , LRG_126:g.28855_28863del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1290-51_1290-43del	ENSP00000513759.1:n.1290-51_1290-43del
ENST00000698509.1:n.1430-51_1430-43del
ENST00000264972.10:c.1290-51_1290-43del MANE Select	ENSP00000264972.5:n.1290-51_1290-43del
ENST00000264972.9:c.1290-51_1290-43del	ENSP00000264972.5:n.1290-51_1290-43del
ENST00000451498.2:c.369-51_369-43del	ENSP00000400475.2:n.369-51_369-43del
ENST00000463643.5:n.1151-51_1151-43del
ENST00000487283.5:n.2342-51_2342-43del
ENST00000495754.1:n.228-51_228-43del
NM_001079.3:c.1290-51_1290-43del , LRG_126t1:c.1290-51_1290-43del	NP_001070.2:n.1290-51_1290-43del
NM_207519.1:c.369-51_369-43del	NP_997402.1:n.369-51_369-43del
XM_005264015.3:c.1272-51_1272-43del	XP_005264072.1:n.1272-51_1272-43del
XM_006712728.2:c.1290-51_1290-43del	XP_006712791.1:n.1290-51_1290-43del
XM_011511783.1:c.1290-51_1290-43del	XP_011510085.1:n.1290-51_1290-43del
XR_923018.1:n.1492-51_1492-43del
XR_923019.1:n.1492-51_1492-43del
XR_923020.1:n.1492-51_1492-43del
XM_017004867.1:c.1659-51_1659-43del	XP_016860356.1:n.1659-51_1659-43del
XM_017004868.1:c.1641-51_1641-43del	XP_016860357.1:n.1641-51_1641-43del
XM_017004869.1:c.1659-51_1659-43del	XP_016860358.1:n.1659-51_1659-43del
XM_017004870.1:c.1659-51_1659-43del	XP_016860359.1:n.1659-51_1659-43del
XR_001738925.1:n.2898-51_2898-43del
XR_001738926.1:n.2898-51_2898-43del
XR_001738927.1:n.2898-51_2898-43del
NM_001079.4:c.1290-51_1290-43del MANE Select	NP_001070.2:n.1290-51_1290-43del
NM_001378594.1:c.1290-51_1290-43del	NP_001365523.1:n.1290-51_1290-43del
NM_207519.2:c.369-51_369-43del	NP_997402.1:n.369-51_369-43del