Canonical Allele Identifier: CA347806298

Gene: ZAP70

Linked Data

• MyVariant Identifiers: chr2:g.98355857T>C (hg19) ; chr2:g.97739394T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97739394T>C , CM000664.2:g.97739394T>C	GRCh38
NC_000002.11:g.98355857T>C , CM000664.1:g.98355857T>C	GRCh37
NC_000002.10:g.97722289T>C	NCBI36
NG_007727.1:g.30827T>C , LRG_126:g.30827T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1756T>C	ENSP00000513759.1:p.Phe586Leu
ENST00000698509.1:n.1896T>C
ENST00000264972.10:c.1756T>C MANE Select	ENSP00000264972.5:p.Phe586Leu
ENST00000264972.9:c.1756T>C	ENSP00000264972.5:p.Phe586Leu
ENST00000451498.2:c.835T>C	ENSP00000400475.2:p.Phe279Leu
ENST00000463643.5:n.1617T>C
ENST00000487283.5:n.2808T>C
NM_001079.3:c.1756T>C , LRG_126t1:c.1756T>C	NP_001070.2:p.Phe586Leu
NM_207519.1:c.835T>C	NP_997402.1:p.Phe279Leu
XM_005264015.3:c.1738T>C	XP_005264072.1:p.Phe580Leu
XM_011511783.1:c.1736+1287T>C	XP_011510085.1:n.1736+1287T>C
XR_923018.1:n.1938+1287T>C
XR_923019.1:n.1938+1287T>C
XR_923020.1:n.2167T>C
XM_017004867.1:c.2125T>C	XP_016860356.1:p.Phe709Leu
XM_017004868.1:c.2107T>C	XP_016860357.1:p.Phe703Leu
XM_017004869.1:c.2105+1287T>C	XP_016860358.1:n.2105+1287T>C
XR_001738925.1:n.3344+1287T>C
XR_001738926.1:n.3344+1287T>C
XR_001738927.1:n.3573T>C
NM_001079.4:c.1756T>C MANE Select	NP_001070.2:p.Phe586Leu
NM_001378594.1:c.1756T>C	NP_001365523.1:p.Phe586Leu
NM_207519.2:c.835T>C	NP_997402.1:p.Phe279Leu