Canonical Allele Identifier: CA361958954

Gene: ITK

Linked Data

• MyVariant Identifiers: chr5:g.156668691G>A (hg19) ; chr5:g.157241681G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157241681G>A , CM000667.2:g.157241681G>A	GRCh38
NC_000005.9:g.156668691G>A , CM000667.1:g.156668691G>A	GRCh37
NC_000005.8:g.156601269G>A	NCBI36
NG_016276.1:g.65785G>A , LRG_189:g.65785G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696962.1:c.887G>A	ENSP00000513001.1:p.Trp296Ter
ENST00000422843.8:c.1021G>A MANE Select	ENSP00000398655.4:p.Gly341Arg
ENST00000422843.7:c.1021G>A	ENSP00000398655.3:p.Gly341Arg
ENST00000519402.5:n.2606G>A
ENST00000519749.1:n.91G>A
ENST00000520173.1:n.139G>A
NM_005546.3:c.1021G>A , LRG_189t1:c.1021G>A	NP_005537.3:p.Gly341Arg
XM_017009443.1:c.646G>A	XP_016864932.1:p.Gly216Arg
NM_005546.4:c.1021G>A MANE Select	NP_005537.3:p.Gly341Arg