Canonical Allele Identifier: CA2660263320

Gene: ZAP70

Linked Data

• gnomAD v4: 2-97739262-ACTTTCTGAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97739264_97739272del , CM000664.2:g.97739264_97739272del	GRCh38
NC_000002.11:g.98355727_98355735del , CM000664.1:g.98355727_98355735del	GRCh37
NC_000002.10:g.97722159_97722167del	NCBI36
NG_007727.1:g.30697_30705del , LRG_126:g.30697_30705del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1737-111_1737-103del	ENSP00000513759.1:n.1737-111_1737-103del
ENST00000698509.1:n.1877-111_1877-103del
ENST00000264972.10:c.1737-111_1737-103del MANE Select	ENSP00000264972.5:n.1737-111_1737-103del
ENST00000264972.9:c.1737-111_1737-103del	ENSP00000264972.5:n.1737-111_1737-103del
ENST00000451498.2:c.816-111_816-103del	ENSP00000400475.2:n.816-111_816-103del
ENST00000463643.5:n.1598-111_1598-103del
ENST00000487283.5:n.2789-111_2789-103del
NM_001079.3:c.1737-111_1737-103del , LRG_126t1:c.1737-111_1737-103del	NP_001070.2:n.1737-111_1737-103del
NM_207519.1:c.816-111_816-103del	NP_997402.1:n.816-111_816-103del
XM_005264015.3:c.1719-111_1719-103del	XP_005264072.1:n.1719-111_1719-103del
XM_011511783.1:c.1736+1157_1736+1165del	XP_011510085.1:n.1736+1157_1736+1165del
XR_923018.1:n.1938+1157_1938+1165del
XR_923019.1:n.1938+1157_1938+1165del
XR_923020.1:n.2148-111_2148-103del
XM_017004867.1:c.2106-111_2106-103del	XP_016860356.1:n.2106-111_2106-103del
XM_017004868.1:c.2088-111_2088-103del	XP_016860357.1:n.2088-111_2088-103del
XM_017004869.1:c.2105+1157_2105+1165del	XP_016860358.1:n.2105+1157_2105+1165del
XR_001738925.1:n.3344+1157_3344+1165del
XR_001738926.1:n.3344+1157_3344+1165del
XR_001738927.1:n.3554-111_3554-103del
NM_001079.4:c.1737-111_1737-103del MANE Select	NP_001070.2:n.1737-111_1737-103del
NM_001378594.1:c.1737-111_1737-103del	NP_001365523.1:n.1737-111_1737-103del
NM_207519.2:c.816-111_816-103del	NP_997402.1:n.816-111_816-103del