Canonical Allele Identifier: CA1594081667
Gene: ITK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157241333C= , CM000667.2:g.157241333C= GRCh38
NC_000005.9:g.156668343C= , CM000667.1:g.156668343C= GRCh37
NC_000005.8:g.156600921C= NCBI36
NG_016276.1:g.65437C= , LRG_189:g.65437C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696962.1:c.852-313C= ENSP00000513001.1:n.852-313C=
ENST00000422843.8:c.986-313C= MANE Select ENSP00000398655.4:n.986-313C=
ENST00000422843.7:c.986-313C= ENSP00000398655.3:n.986-313C=
ENST00000519402.5:n.2258C=
ENST00000520173.1:n.104-313C=
NM_005546.3:c.986-313C= , LRG_189t1:c.986-313C= NP_005537.3:n.986-313C=
XM_017009443.1:c.611-313C= XP_016864932.1:n.611-313C=
NM_005546.4:c.986-313C= MANE Select NP_005537.3:n.986-313C=