Canonical Allele Identifier: CA347803312

Gene: ZAP70

Linked Data

• MyVariant Identifiers: chr2:g.98353982T>C (hg19) ; chr2:g.97737519T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737519T>C , CM000664.2:g.97737519T>C	GRCh38
NC_000002.11:g.98353982T>C , CM000664.1:g.98353982T>C	GRCh37
NC_000002.10:g.97720414T>C	NCBI36
NG_007727.1:g.28952T>C , LRG_126:g.28952T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1336T>C	ENSP00000513759.1:p.Ser446Pro
ENST00000698509.1:n.1476T>C
ENST00000264972.10:c.1336T>C MANE Select	ENSP00000264972.5:p.Ser446Pro
ENST00000264972.9:c.1336T>C	ENSP00000264972.5:p.Ser446Pro
ENST00000451498.2:c.415T>C	ENSP00000400475.2:p.Ser139Pro
ENST00000463643.5:n.1197T>C
ENST00000487283.5:n.2388T>C
ENST00000495754.1:n.274T>C
NM_001079.3:c.1336T>C , LRG_126t1:c.1336T>C	NP_001070.2:p.Ser446Pro
NM_207519.1:c.415T>C	NP_997402.1:p.Ser139Pro
XM_005264015.3:c.1318T>C	XP_005264072.1:p.Ser440Pro
XM_006712728.2:c.1336T>C	XP_006712791.1:p.Ser446Pro
XM_011511783.1:c.1336T>C	XP_011510085.1:p.Ser446Pro
XR_923018.1:n.1538T>C
XR_923019.1:n.1538T>C
XR_923020.1:n.1538T>C
XM_017004867.1:c.1705T>C	XP_016860356.1:p.Ser569Pro
XM_017004868.1:c.1687T>C	XP_016860357.1:p.Ser563Pro
XM_017004869.1:c.1705T>C	XP_016860358.1:p.Ser569Pro
XM_017004870.1:c.1705T>C	XP_016860359.1:p.Ser569Pro
XR_001738925.1:n.2944T>C
XR_001738926.1:n.2944T>C
XR_001738927.1:n.2944T>C
NM_001079.4:c.1336T>C MANE Select	NP_001070.2:p.Ser446Pro
NM_001378594.1:c.1336T>C	NP_001365523.1:p.Ser446Pro
NM_207519.2:c.415T>C	NP_997402.1:p.Ser139Pro