Canonical Allele Identifier: CA347806275

Gene: ZAP70

Linked Data

• MyVariant Identifiers: chr2:g.98355849G>T (hg19) ; chr2:g.97739386G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97739386G>T , CM000664.2:g.97739386G>T	GRCh38
NC_000002.11:g.98355849G>T , CM000664.1:g.98355849G>T	GRCh37
NC_000002.10:g.97722281G>T	NCBI36
NG_007727.1:g.30819G>T , LRG_126:g.30819G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1748G>T	ENSP00000513759.1:p.Arg583Leu
ENST00000698509.1:n.1888G>T
ENST00000264972.10:c.1748G>T MANE Select	ENSP00000264972.5:p.Arg583Leu
ENST00000264972.9:c.1748G>T	ENSP00000264972.5:p.Arg583Leu
ENST00000451498.2:c.827G>T	ENSP00000400475.2:p.Arg276Leu
ENST00000463643.5:n.1609G>T
ENST00000487283.5:n.2800G>T
NM_001079.3:c.1748G>T , LRG_126t1:c.1748G>T	NP_001070.2:p.Arg583Leu
NM_207519.1:c.827G>T	NP_997402.1:p.Arg276Leu
XM_005264015.3:c.1730G>T	XP_005264072.1:p.Arg577Leu
XM_011511783.1:c.1736+1279G>T	XP_011510085.1:n.1736+1279G>T
XR_923018.1:n.1938+1279G>T
XR_923019.1:n.1938+1279G>T
XR_923020.1:n.2159G>T
XM_017004867.1:c.2117G>T	XP_016860356.1:p.Arg706Leu
XM_017004868.1:c.2099G>T	XP_016860357.1:p.Arg700Leu
XM_017004869.1:c.2105+1279G>T	XP_016860358.1:n.2105+1279G>T
XR_001738925.1:n.3344+1279G>T
XR_001738926.1:n.3344+1279G>T
XR_001738927.1:n.3565G>T
NM_001079.4:c.1748G>T MANE Select	NP_001070.2:p.Arg583Leu
NM_001378594.1:c.1748G>T	NP_001365523.1:p.Arg583Leu
NM_207519.2:c.827G>T	NP_997402.1:p.Arg276Leu