Canonical Allele Identifier: CA1083354587
Gene: ITK HGNC NCBI

Linked Data

dbSNP Id: rs1754892100

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157241318del , CM000667.2:g.157241318del GRCh38
NC_000005.9:g.156668328del , CM000667.1:g.156668328del GRCh37
NC_000005.8:g.156600906del NCBI36
NG_016276.1:g.65422del , LRG_189:g.65422del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696962.1:c.852-328del ENSP00000513001.1:n.852-328del
ENST00000422843.8:c.986-328del MANE Select ENSP00000398655.4:n.986-328del
ENST00000422843.7:c.986-328del ENSP00000398655.3:n.986-328del
ENST00000519402.5:n.2243del
ENST00000520173.1:n.104-328del
NM_005546.3:c.986-328del , LRG_189t1:c.986-328del NP_005537.3:n.986-328del
XM_017009443.1:c.611-328del XP_016864932.1:n.611-328del
NM_005546.4:c.986-328del MANE Select NP_005537.3:n.986-328del