Canonical Allele Identifier: CA361958951
Gene: ITK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157241680T>G , CM000667.2:g.157241680T>G GRCh38
NC_000005.9:g.156668690T>G , CM000667.1:g.156668690T>G GRCh37
NC_000005.8:g.156601268T>G NCBI36
NG_016276.1:g.65784T>G , LRG_189:g.65784T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696962.1:c.886T>G ENSP00000513001.1:p.Trp296Gly
ENST00000422843.8:c.1020T>G MANE Select ENSP00000398655.4:p.Phe340Leu
ENST00000422843.7:c.1020T>G ENSP00000398655.3:p.Phe340Leu
ENST00000519402.5:n.2605T>G
ENST00000519749.1:n.90T>G
ENST00000520173.1:n.138T>G
NM_005546.3:c.1020T>G , LRG_189t1:c.1020T>G NP_005537.3:p.Phe340Leu
XM_017009443.1:c.645T>G XP_016864932.1:p.Phe215Leu
NM_005546.4:c.1020T>G MANE Select NP_005537.3:p.Phe340Leu