Canonical Allele Identifier: CA361958979
Gene: ITK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157241689G>C , CM000667.2:g.157241689G>C GRCh38
NC_000005.9:g.156668699G>C , CM000667.1:g.156668699G>C GRCh37
NC_000005.8:g.156601277G>C NCBI36
NG_016276.1:g.65793G>C , LRG_189:g.65793G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696962.1:c.895G>C ENSP00000513001.1:p.Glu299Gln
ENST00000422843.8:c.1029G>C MANE Select ENSP00000398655.4:p.Gln343His
ENST00000422843.7:c.1029G>C ENSP00000398655.3:p.Gln343His
ENST00000519402.5:n.2614G>C
ENST00000519749.1:n.99G>C
ENST00000520173.1:n.147G>C
NM_005546.3:c.1029G>C , LRG_189t1:c.1029G>C NP_005537.3:p.Gln343His
XM_017009443.1:c.654G>C XP_016864932.1:p.Gln218His
NM_005546.4:c.1029G>C MANE Select NP_005537.3:p.Gln343His