Canonical Allele Identifier: CA347806254

Gene: ZAP70

Linked Data

• MyVariant Identifiers: chr2:g.98355845G>C (hg19) ; chr2:g.97739382G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97739382G>C , CM000664.2:g.97739382G>C	GRCh38
NC_000002.11:g.98355845G>C , CM000664.1:g.98355845G>C	GRCh37
NC_000002.10:g.97722277G>C	NCBI36
NG_007727.1:g.30815G>C , LRG_126:g.30815G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1744G>C	ENSP00000513759.1:p.Asp582His
ENST00000698509.1:n.1884G>C
ENST00000264972.10:c.1744G>C MANE Select	ENSP00000264972.5:p.Asp582His
ENST00000264972.9:c.1744G>C	ENSP00000264972.5:p.Asp582His
ENST00000451498.2:c.823G>C	ENSP00000400475.2:p.Asp275His
ENST00000463643.5:n.1605G>C
ENST00000487283.5:n.2796G>C
NM_001079.3:c.1744G>C , LRG_126t1:c.1744G>C	NP_001070.2:p.Asp582His
NM_207519.1:c.823G>C	NP_997402.1:p.Asp275His
XM_005264015.3:c.1726G>C	XP_005264072.1:p.Asp576His
XM_011511783.1:c.1736+1275G>C	XP_011510085.1:n.1736+1275G>C
XR_923018.1:n.1938+1275G>C
XR_923019.1:n.1938+1275G>C
XR_923020.1:n.2155G>C
XM_017004867.1:c.2113G>C	XP_016860356.1:p.Asp705His
XM_017004868.1:c.2095G>C	XP_016860357.1:p.Asp699His
XM_017004869.1:c.2105+1275G>C	XP_016860358.1:n.2105+1275G>C
XR_001738925.1:n.3344+1275G>C
XR_001738926.1:n.3344+1275G>C
XR_001738927.1:n.3561G>C
NM_001079.4:c.1744G>C MANE Select	NP_001070.2:p.Asp582His
NM_001378594.1:c.1744G>C	NP_001365523.1:p.Asp582His
NM_207519.2:c.823G>C	NP_997402.1:p.Asp275His