Canonical Allele Identifier: CA2676197014

Gene: ITK

Linked Data

• gnomAD v4: 5-157241601-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157241601G>T , CM000667.2:g.157241601G>T	GRCh38
NC_000005.9:g.156668611G>T , CM000667.1:g.156668611G>T	GRCh37
NC_000005.8:g.156601189G>T	NCBI36
NG_016276.1:g.65705G>T , LRG_189:g.65705G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696962.1:c.852-45G>T	ENSP00000513001.1:n.852-45G>T
ENST00000422843.8:c.986-45G>T MANE Select	ENSP00000398655.4:n.986-45G>T
ENST00000422843.7:c.986-45G>T	ENSP00000398655.3:n.986-45G>T
ENST00000519402.5:n.2526G>T
ENST00000519749.1:n.11G>T
ENST00000520173.1:n.104-45G>T
NM_005546.3:c.986-45G>T , LRG_189t1:c.986-45G>T	NP_005537.3:n.986-45G>T
XM_017009443.1:c.611-45G>T	XP_016864932.1:n.611-45G>T
NM_005546.4:c.986-45G>T MANE Select	NP_005537.3:n.986-45G>T