Canonical Allele Identifier: CA347803238

Gene: ZAP70

Linked Data

• MyVariant Identifiers: chr2:g.98353946C>G (hg19) ; chr2:g.97737483C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737483C>G , CM000664.2:g.97737483C>G	GRCh38
NC_000002.11:g.98353946C>G , CM000664.1:g.98353946C>G	GRCh37
NC_000002.10:g.97720378C>G	NCBI36
NG_007727.1:g.28916C>G , LRG_126:g.28916C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698508.1:c.1300C>G	ENSP00000513759.1:p.Pro434Ala
ENST00000698509.1:n.1440C>G
ENST00000264972.10:c.1300C>G MANE Select	ENSP00000264972.5:p.Pro434Ala
ENST00000264972.9:c.1300C>G	ENSP00000264972.5:p.Pro434Ala
ENST00000451498.2:c.379C>G	ENSP00000400475.2:p.Pro127Ala
ENST00000463643.5:n.1161C>G
ENST00000487283.5:n.2352C>G
ENST00000495754.1:n.238C>G
NM_001079.3:c.1300C>G , LRG_126t1:c.1300C>G	NP_001070.2:p.Pro434Ala
NM_207519.1:c.379C>G	NP_997402.1:p.Pro127Ala
XM_005264015.3:c.1282C>G	XP_005264072.1:p.Pro428Ala
XM_006712728.2:c.1300C>G	XP_006712791.1:p.Pro434Ala
XM_011511783.1:c.1300C>G	XP_011510085.1:p.Pro434Ala
XR_923018.1:n.1502C>G
XR_923019.1:n.1502C>G
XR_923020.1:n.1502C>G
XM_017004867.1:c.1669C>G	XP_016860356.1:p.Pro557Ala
XM_017004868.1:c.1651C>G	XP_016860357.1:p.Pro551Ala
XM_017004869.1:c.1669C>G	XP_016860358.1:p.Pro557Ala
XM_017004870.1:c.1669C>G	XP_016860359.1:p.Pro557Ala
XR_001738925.1:n.2908C>G
XR_001738926.1:n.2908C>G
XR_001738927.1:n.2908C>G
NM_001079.4:c.1300C>G MANE Select	NP_001070.2:p.Pro434Ala
NM_001378594.1:c.1300C>G	NP_001365523.1:p.Pro434Ala
NM_207519.2:c.379C>G	NP_997402.1:p.Pro127Ala