Canonical Allele Identifier: CA2660263366

Gene: ZAP70

Linked Data

• gnomAD v4: 2-97739310-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97739313del , CM000664.2:g.97739313del	GRCh38
NC_000002.11:g.98355776del , CM000664.1:g.98355776del	GRCh37
NC_000002.10:g.97722208del	NCBI36
NG_007727.1:g.30746del , LRG_126:g.30746del

Transcript Alleles

HGVS	Amino-acid change
ENST00000698508.1:c.1737-62del	ENSP00000513759.1:n.1737-62del
ENST00000698509.1:n.1877-62del
ENST00000264972.10:c.1737-62del MANE Select	ENSP00000264972.5:n.1737-62del
ENST00000264972.9:c.1737-62del	ENSP00000264972.5:n.1737-62del
ENST00000451498.2:c.816-62del	ENSP00000400475.2:n.816-62del
ENST00000463643.5:n.1598-62del
ENST00000487283.5:n.2789-62del
NM_001079.3:c.1737-62del , LRG_126t1:c.1737-62del	NP_001070.2:n.1737-62del
NM_207519.1:c.816-62del	NP_997402.1:n.816-62del
XM_005264015.3:c.1719-62del	XP_005264072.1:n.1719-62del
XM_011511783.1:c.1736+1206del	XP_011510085.1:n.1736+1206del
XR_923018.1:n.1938+1206del
XR_923019.1:n.1938+1206del
XR_923020.1:n.2148-62del
XM_017004867.1:c.2106-62del	XP_016860356.1:n.2106-62del
XM_017004868.1:c.2088-62del	XP_016860357.1:n.2088-62del
XM_017004869.1:c.2105+1206del	XP_016860358.1:n.2105+1206del
XR_001738925.1:n.3344+1206del
XR_001738926.1:n.3344+1206del
XR_001738927.1:n.3554-62del
NM_001079.4:c.1737-62del MANE Select	NP_001070.2:n.1737-62del
NM_001378594.1:c.1737-62del	NP_001365523.1:n.1737-62del
NM_207519.2:c.816-62del	NP_997402.1:n.816-62del