Canonical Allele Identifier: CA1273122613

Gene: ZAP70

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97738085A= , CM000664.2:g.97738085A=	GRCh38
NC_000002.11:g.98354548A= , CM000664.1:g.98354548A=	GRCh37
NC_000002.10:g.97720980A=	NCBI36
NG_007727.1:g.29518A= , LRG_126:g.29518A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1714A=	ENSP00000513759.1:p.Met572=
ENST00000698509.1:n.1854A=
ENST00000264972.10:c.1714A= MANE Select	ENSP00000264972.5:p.Met572=
ENST00000264972.9:c.1714A=	ENSP00000264972.5:p.Met572=
ENST00000451498.2:c.793A=	ENSP00000400475.2:p.Met265=
ENST00000463643.5:n.1575A=
ENST00000487283.5:n.2766A=
ENST00000489250.1:n.167A=
NM_001079.3:c.1714A= , LRG_126t1:c.1714A=	NP_001070.2:p.Met572=
NM_207519.1:c.793A=	NP_997402.1:p.Met265=
XM_005264015.3:c.1696A=	XP_005264072.1:p.Met566=
XM_006712728.2:c.1714A=	XP_006712791.1:p.Met572=
XM_011511783.1:c.1714A=	XP_011510085.1:p.Met572=
XR_923018.1:n.1916A=
XR_923019.1:n.1916A=
XR_923020.1:n.1916A=
XM_017004867.1:c.2083A=	XP_016860356.1:p.Met695=
XM_017004868.1:c.2065A=	XP_016860357.1:p.Met689=
XM_017004869.1:c.2083A=	XP_016860358.1:p.Met695=
XM_017004870.1:c.2083A=	XP_016860359.1:p.Met695=
XR_001738925.1:n.3322A=
XR_001738926.1:n.3322A=
XR_001738927.1:n.3322A=
NM_001079.4:c.1714A= MANE Select	NP_001070.2:p.Met572=
NM_001378594.1:c.1714A=	NP_001365523.1:p.Met572=
NM_207519.2:c.793A=	NP_997402.1:p.Met265=