Canonical Allele Identifier: CA2578466352
Gene: ITK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157241602_157241603del , CM000667.2:g.157241602_157241603del GRCh38
NC_000005.9:g.156668612_156668613del , CM000667.1:g.156668612_156668613del GRCh37
NC_000005.8:g.156601190_156601191del NCBI36
NG_016276.1:g.65706_65707del , LRG_189:g.65706_65707del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696962.1:c.852-44_852-43del ENSP00000513001.1:n.852-44_852-43del
ENST00000422843.8:c.986-44_986-43del MANE Select ENSP00000398655.4:n.986-44_986-43del
ENST00000422843.7:c.986-44_986-43del ENSP00000398655.3:n.986-44_986-43del
ENST00000519402.5:n.2527_2528del
ENST00000519749.1:n.12_13del
ENST00000520173.1:n.104-44_104-43del
NM_005546.3:c.986-44_986-43del , LRG_189t1:c.986-44_986-43del NP_005537.3:n.986-44_986-43del
XM_017009443.1:c.611-44_611-43del XP_016864932.1:n.611-44_611-43del
NM_005546.4:c.986-44_986-43del MANE Select NP_005537.3:n.986-44_986-43del