Canonical Allele Identifier: CA347806279

Gene: ZAP70

Linked Data

• MyVariant Identifiers: chr2:g.98355851C>G (hg19) ; chr2:g.97739388C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97739388C>G , CM000664.2:g.97739388C>G	GRCh38
NC_000002.11:g.98355851C>G , CM000664.1:g.98355851C>G	GRCh37
NC_000002.10:g.97722283C>G	NCBI36
NG_007727.1:g.30821C>G , LRG_126:g.30821C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1750C>G	ENSP00000513759.1:p.Pro584Ala
ENST00000698509.1:n.1890C>G
ENST00000264972.10:c.1750C>G MANE Select	ENSP00000264972.5:p.Pro584Ala
ENST00000264972.9:c.1750C>G	ENSP00000264972.5:p.Pro584Ala
ENST00000451498.2:c.829C>G	ENSP00000400475.2:p.Pro277Ala
ENST00000463643.5:n.1611C>G
ENST00000487283.5:n.2802C>G
NM_001079.3:c.1750C>G , LRG_126t1:c.1750C>G	NP_001070.2:p.Pro584Ala
NM_207519.1:c.829C>G	NP_997402.1:p.Pro277Ala
XM_005264015.3:c.1732C>G	XP_005264072.1:p.Pro578Ala
XM_011511783.1:c.1736+1281C>G	XP_011510085.1:n.1736+1281C>G
XR_923018.1:n.1938+1281C>G
XR_923019.1:n.1938+1281C>G
XR_923020.1:n.2161C>G
XM_017004867.1:c.2119C>G	XP_016860356.1:p.Pro707Ala
XM_017004868.1:c.2101C>G	XP_016860357.1:p.Pro701Ala
XM_017004869.1:c.2105+1281C>G	XP_016860358.1:n.2105+1281C>G
XR_001738925.1:n.3344+1281C>G
XR_001738926.1:n.3344+1281C>G
XR_001738927.1:n.3567C>G
NM_001079.4:c.1750C>G MANE Select	NP_001070.2:p.Pro584Ala
NM_001378594.1:c.1750C>G	NP_001365523.1:p.Pro584Ala
NM_207519.2:c.829C>G	NP_997402.1:p.Pro277Ala