Canonical Allele Identifier: CA447431344
Gene: ITK HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.156668699G>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000696962.1:c.895G>A ENSP00000513001.1:p.Glu299Lys
ENST00000422843.8:c.1029G>A MANE Select ENSP00000398655.4:p.Gln343=
ENST00000422843.7:c.1029G>A ENSP00000398655.3:p.Gln343=
ENST00000519402.5:n.2614G>A
ENST00000519749.1:n.99G>A
ENST00000520173.1:n.147G>A
NM_005546.3:c.1029G>A , LRG_189t1:c.1029G>A NP_005537.3:p.Gln343=
XM_017009443.1:c.654G>A XP_016864932.1:p.Gln218=
NM_005546.4:c.1029G>A MANE Select NP_005537.3:p.Gln343=