Canonical Allele Identifier: CA347803294

Gene: ZAP70

Linked Data

• MyVariant Identifiers: chr2:g.98353974A>C (hg19) ; chr2:g.97737511A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737511A>C , CM000664.2:g.97737511A>C	GRCh38
NC_000002.11:g.98353974A>C , CM000664.1:g.98353974A>C	GRCh37
NC_000002.10:g.97720406A>C	NCBI36
NG_007727.1:g.28944A>C , LRG_126:g.28944A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1328A>C	ENSP00000513759.1:p.His443Pro
ENST00000698509.1:n.1468A>C
ENST00000264972.10:c.1328A>C MANE Select	ENSP00000264972.5:p.His443Pro
ENST00000264972.9:c.1328A>C	ENSP00000264972.5:p.His443Pro
ENST00000451498.2:c.407A>C	ENSP00000400475.2:p.His136Pro
ENST00000463643.5:n.1189A>C
ENST00000487283.5:n.2380A>C
ENST00000495754.1:n.266A>C
NM_001079.3:c.1328A>C , LRG_126t1:c.1328A>C	NP_001070.2:p.His443Pro
NM_207519.1:c.407A>C	NP_997402.1:p.His136Pro
XM_005264015.3:c.1310A>C	XP_005264072.1:p.His437Pro
XM_006712728.2:c.1328A>C	XP_006712791.1:p.His443Pro
XM_011511783.1:c.1328A>C	XP_011510085.1:p.His443Pro
XR_923018.1:n.1530A>C
XR_923019.1:n.1530A>C
XR_923020.1:n.1530A>C
XM_017004867.1:c.1697A>C	XP_016860356.1:p.His566Pro
XM_017004868.1:c.1679A>C	XP_016860357.1:p.His560Pro
XM_017004869.1:c.1697A>C	XP_016860358.1:p.His566Pro
XM_017004870.1:c.1697A>C	XP_016860359.1:p.His566Pro
XR_001738925.1:n.2936A>C
XR_001738926.1:n.2936A>C
XR_001738927.1:n.2936A>C
NM_001079.4:c.1328A>C MANE Select	NP_001070.2:p.His443Pro
NM_001378594.1:c.1328A>C	NP_001365523.1:p.His443Pro
NM_207519.2:c.407A>C	NP_997402.1:p.His136Pro