Canonical Allele Identifier: CA1594081652
Gene: ITK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157241297C= , CM000667.2:g.157241297C= GRCh38
NC_000005.9:g.156668307C= , CM000667.1:g.156668307C= GRCh37
NC_000005.8:g.156600885C= NCBI36
NG_016276.1:g.65401C= , LRG_189:g.65401C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696962.1:c.852-349C= ENSP00000513001.1:n.852-349C=
ENST00000422843.8:c.986-349C= MANE Select ENSP00000398655.4:n.986-349C=
ENST00000422843.7:c.986-349C= ENSP00000398655.3:n.986-349C=
ENST00000519402.5:n.2222C=
ENST00000520173.1:n.104-349C=
NM_005546.3:c.986-349C= , LRG_189t1:c.986-349C= NP_005537.3:n.986-349C=
XM_017009443.1:c.611-349C= XP_016864932.1:n.611-349C=
NM_005546.4:c.986-349C= MANE Select NP_005537.3:n.986-349C=