Canonical Allele Identifier: CA427556331

Gene: ZAP70

Linked Data

• dbSNP Id: rs199775081
• MyVariant Identifiers: chr2:g.98353967C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737504C>T , CM000664.2:g.97737504C>T	GRCh38
NC_000002.11:g.98353967C>T , CM000664.1:g.98353967C>T	GRCh37
NC_000002.10:g.97720399C>T	NCBI36
NG_007727.1:g.28937C>T , LRG_126:g.28937C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1321C>T	ENSP00000513759.1:p.Leu441=
ENST00000698509.1:n.1461C>T
ENST00000264972.10:c.1321C>T MANE Select	ENSP00000264972.5:p.Leu441=
ENST00000264972.9:c.1321C>T	ENSP00000264972.5:p.Leu441=
ENST00000451498.2:c.400C>T	ENSP00000400475.2:p.Leu134=
ENST00000463643.5:n.1182C>T
ENST00000487283.5:n.2373C>T
ENST00000495754.1:n.259C>T
NM_001079.3:c.1321C>T , LRG_126t1:c.1321C>T	NP_001070.2:p.Leu441=
NM_207519.1:c.400C>T	NP_997402.1:p.Leu134=
XM_005264015.3:c.1303C>T	XP_005264072.1:p.Leu435=
XM_006712728.2:c.1321C>T	XP_006712791.1:p.Leu441=
XM_011511783.1:c.1321C>T	XP_011510085.1:p.Leu441=
XR_923018.1:n.1523C>T
XR_923019.1:n.1523C>T
XR_923020.1:n.1523C>T
XM_017004867.1:c.1690C>T	XP_016860356.1:p.Leu564=
XM_017004868.1:c.1672C>T	XP_016860357.1:p.Leu558=
XM_017004869.1:c.1690C>T	XP_016860358.1:p.Leu564=
XM_017004870.1:c.1690C>T	XP_016860359.1:p.Leu564=
XR_001738925.1:n.2929C>T
XR_001738926.1:n.2929C>T
XR_001738927.1:n.2929C>T
NM_001079.4:c.1321C>T MANE Select	NP_001070.2:p.Leu441=
NM_001378594.1:c.1321C>T	NP_001365523.1:p.Leu441=
NM_207519.2:c.400C>T	NP_997402.1:p.Leu134=