Canonical Allele Identifier: CA347806392

Gene: ZAP70

Linked Data

• MyVariant Identifiers: chr2:g.98355879T>A (hg19) ; chr2:g.97739416T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97739416T>A , CM000664.2:g.97739416T>A	GRCh38
NC_000002.11:g.98355879T>A , CM000664.1:g.98355879T>A	GRCh37
NC_000002.10:g.97722311T>A	NCBI36
NG_007727.1:g.30849T>A , LRG_126:g.30849T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1778T>A	ENSP00000513759.1:p.Met593Lys
ENST00000698509.1:n.1918T>A
ENST00000264972.10:c.1778T>A MANE Select	ENSP00000264972.5:p.Met593Lys
ENST00000264972.9:c.1778T>A	ENSP00000264972.5:p.Met593Lys
ENST00000451498.2:c.857T>A	ENSP00000400475.2:p.Met286Lys
ENST00000463643.5:n.1639T>A
ENST00000487283.5:n.2830T>A
NM_001079.3:c.1778T>A , LRG_126t1:c.1778T>A	NP_001070.2:p.Met593Lys
NM_207519.1:c.857T>A	NP_997402.1:p.Met286Lys
XM_005264015.3:c.1760T>A	XP_005264072.1:p.Met587Lys
XM_011511783.1:c.1736+1309T>A	XP_011510085.1:n.1736+1309T>A
XR_923018.1:n.1938+1309T>A
XR_923019.1:n.1938+1309T>A
XR_923020.1:n.2189T>A
XM_017004867.1:c.2147T>A	XP_016860356.1:p.Met716Lys
XM_017004868.1:c.2129T>A	XP_016860357.1:p.Met710Lys
XM_017004869.1:c.2105+1309T>A	XP_016860358.1:n.2105+1309T>A
XR_001738925.1:n.3344+1309T>A
XR_001738926.1:n.3344+1309T>A
XR_001738927.1:n.3595T>A
NM_001079.4:c.1778T>A MANE Select	NP_001070.2:p.Met593Lys
NM_001378594.1:c.1778T>A	NP_001365523.1:p.Met593Lys
NM_207519.2:c.857T>A	NP_997402.1:p.Met286Lys