Canonical Allele Identifier: CA1594081780
Gene: ITK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157241605A= , CM000667.2:g.157241605A= GRCh38
NC_000005.9:g.156668615A= , CM000667.1:g.156668615A= GRCh37
NC_000005.8:g.156601193A= NCBI36
NG_016276.1:g.65709A= , LRG_189:g.65709A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696962.1:c.852-41A= ENSP00000513001.1:n.852-41A=
ENST00000422843.8:c.986-41A= MANE Select ENSP00000398655.4:n.986-41A=
ENST00000422843.7:c.986-41A= ENSP00000398655.3:n.986-41A=
ENST00000519402.5:n.2530A=
ENST00000519749.1:n.15A=
ENST00000520173.1:n.104-41A=
NM_005546.3:c.986-41A= , LRG_189t1:c.986-41A= NP_005537.3:n.986-41A=
XM_017009443.1:c.611-41A= XP_016864932.1:n.611-41A=
NM_005546.4:c.986-41A= MANE Select NP_005537.3:n.986-41A=