Canonical Allele Identifier: CA427556319

Gene: ZAP70

Linked Data

• gnomAD v4: 2-97737485-T-C
• MyVariant Identifiers: chr2:g.98353948T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737485T>C , CM000664.2:g.97737485T>C	GRCh38
NC_000002.11:g.98353948T>C , CM000664.1:g.98353948T>C	GRCh37
NC_000002.10:g.97720380T>C	NCBI36
NG_007727.1:g.28918T>C , LRG_126:g.28918T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698508.1:c.1302T>C	ENSP00000513759.1:p.Pro434=
ENST00000698509.1:n.1442T>C
ENST00000264972.10:c.1302T>C MANE Select	ENSP00000264972.5:p.Pro434=
ENST00000264972.9:c.1302T>C	ENSP00000264972.5:p.Pro434=
ENST00000451498.2:c.381T>C	ENSP00000400475.2:p.Pro127=
ENST00000463643.5:n.1163T>C
ENST00000487283.5:n.2354T>C
ENST00000495754.1:n.240T>C
NM_001079.3:c.1302T>C , LRG_126t1:c.1302T>C	NP_001070.2:p.Pro434=
NM_207519.1:c.381T>C	NP_997402.1:p.Pro127=
XM_005264015.3:c.1284T>C	XP_005264072.1:p.Pro428=
XM_006712728.2:c.1302T>C	XP_006712791.1:p.Pro434=
XM_011511783.1:c.1302T>C	XP_011510085.1:p.Pro434=
XR_923018.1:n.1504T>C
XR_923019.1:n.1504T>C
XR_923020.1:n.1504T>C
XM_017004867.1:c.1671T>C	XP_016860356.1:p.Pro557=
XM_017004868.1:c.1653T>C	XP_016860357.1:p.Pro551=
XM_017004869.1:c.1671T>C	XP_016860358.1:p.Pro557=
XM_017004870.1:c.1671T>C	XP_016860359.1:p.Pro557=
XR_001738925.1:n.2910T>C
XR_001738926.1:n.2910T>C
XR_001738927.1:n.2910T>C
NM_001079.4:c.1302T>C MANE Select	NP_001070.2:p.Pro434=
NM_001378594.1:c.1302T>C	NP_001365523.1:p.Pro434=
NM_207519.2:c.381T>C	NP_997402.1:p.Pro127=