Canonical Allele Identifier: CA130157698
Gene: ITK HGNC NCBI

Linked Data

dbSNP Id: rs772818539
gnomAD v2: 5-156668320-T-TA
gnomAD v3: 5-157241310-T-TA
gnomAD v4: 5-157241310-T-TA
MyVariant Identifiers: chr5:g.156668320_156668321insA (hg19) chr5:g.157241310_157241311insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157241312dup , CM000667.2:g.157241312dup GRCh38
NC_000005.9:g.156668322dup , CM000667.1:g.156668322dup GRCh37
NC_000005.8:g.156600900dup NCBI36
NG_016276.1:g.65416dup , LRG_189:g.65416dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696962.1:c.852-334dup ENSP00000513001.1:n.852-334dup
ENST00000422843.8:c.986-334dup MANE Select ENSP00000398655.4:n.986-334dup
ENST00000422843.7:c.986-334dup ENSP00000398655.3:n.986-334dup
ENST00000519402.5:n.2237dup
ENST00000520173.1:n.104-334dup
NM_005546.3:c.986-334dup , LRG_189t1:c.986-334dup NP_005537.3:n.986-334dup
XM_017009443.1:c.611-334dup XP_016864932.1:n.611-334dup
NM_005546.4:c.986-334dup MANE Select NP_005537.3:n.986-334dup
Search 100 bp 5'
Search 100 bp 3'