Canonical Allele Identifier: CA361958893
Gene: ITK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157241666T>G , CM000667.2:g.157241666T>G GRCh38
NC_000005.9:g.156668676T>G , CM000667.1:g.156668676T>G GRCh37
NC_000005.8:g.156601254T>G NCBI36
NG_016276.1:g.65770T>G , LRG_189:g.65770T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696962.1:c.872T>G ENSP00000513001.1:p.Val291Gly
ENST00000422843.8:c.1006T>G MANE Select ENSP00000398655.4:p.Tyr336Asp
ENST00000422843.7:c.1006T>G ENSP00000398655.3:p.Tyr336Asp
ENST00000519402.5:n.2591T>G
ENST00000519749.1:n.76T>G
ENST00000520173.1:n.124T>G
NM_005546.3:c.1006T>G , LRG_189t1:c.1006T>G NP_005537.3:p.Tyr336Asp
XM_017009443.1:c.631T>G XP_016864932.1:p.Tyr211Asp
NM_005546.4:c.1006T>G MANE Select NP_005537.3:p.Tyr336Asp