Canonical Allele Identifier: CA2581505878
Gene: ITK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157181989G>C , CM000667.2:g.157181989G>C GRCh38
NC_000005.9:g.156609000G>C , CM000667.1:g.156609000G>C GRCh37
NC_000005.8:g.156541578G>C NCBI36
NG_016276.1:g.6094G>C , LRG_189:g.6094G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696962.1:c.138+874G>C ENSP00000513001.1:n.138+874G>C
ENST00000422843.8:c.138+874G>C MANE Select ENSP00000398655.4:n.138+874G>C
ENST00000422843.7:c.138+874G>C ENSP00000398655.3:n.138+874G>C
ENST00000517779.1:c.138+874G>C ENSP00000431054.1:n.138+874G>C
ENST00000519402.5:n.273+874G>C
ENST00000520555.5:n.276+874G>C
ENST00000521769.5:c.-238+15843G>C ENSP00000430327.1:n.-238+15843G>C
ENST00000522616.1:n.279+874G>C
NM_005546.3:c.138+874G>C , LRG_189t1:c.138+874G>C NP_005537.3:n.138+874G>C
NM_005546.4:c.138+874G>C MANE Select NP_005537.3:n.138+874G>C