Canonical Allele Identifier: CA2676196813
Gene: ITK HGNC NCBI

Linked Data

gnomAD v4: 5-157241296-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157241296C>A , CM000667.2:g.157241296C>A GRCh38
NC_000005.9:g.156668306C>A , CM000667.1:g.156668306C>A GRCh37
NC_000005.8:g.156600884C>A NCBI36
NG_016276.1:g.65400C>A , LRG_189:g.65400C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696962.1:c.852-350C>A ENSP00000513001.1:n.852-350C>A
ENST00000422843.8:c.986-350C>A MANE Select ENSP00000398655.4:n.986-350C>A
ENST00000422843.7:c.986-350C>A ENSP00000398655.3:n.986-350C>A
ENST00000519402.5:n.2221C>A
ENST00000520173.1:n.104-350C>A
NM_005546.3:c.986-350C>A , LRG_189t1:c.986-350C>A NP_005537.3:n.986-350C>A
XM_017009443.1:c.611-350C>A XP_016864932.1:n.611-350C>A
NM_005546.4:c.986-350C>A MANE Select NP_005537.3:n.986-350C>A
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