Canonical Allele Identifier: CA8474847
Gene: TAOK1 HGNC NCBI

Linked Data

dbSNP Id: rs767760692
ExAC: 17:27861113 T / TC
gnomAD v2: 17-27861113-T-TC
gnomAD v3: 17-29534095-T-TC
gnomAD v4: 17-29534095-T-TC
MyVariant Identifiers: chr17:g.27861113_27861114insC (hg19) chr17:g.27861114_27861115delinsCTC (hg19) chr17:g.27861114_27861117delinsCTCTC (hg19) chr17:g.29534095_29534096insC (hg38) chr17:g.29534096_29534097delinsCTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29534095_29534096insC , CM000679.2:g.29534095_29534096insC GRCh38
NC_000017.10:g.27861113_27861114insC , CM000679.1:g.27861113_27861114insC GRCh37
NC_000017.9:g.24885239_24885240insC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261716.8:c.2362-23_2362-22insC MANE Select ENSP00000261716.3:n.2362-23_2362-22insC
ENST00000261716.7:c.2362-23_2362-22insC ENSP00000261716.3:n.2362-23_2362-22insC
ENST00000536202.1:c.1918-23_1918-22insC ENSP00000438819.1:n.1918-23_1918-22insC
NM_020791.2:c.2362-23_2362-22insC NP_065842.1:n.2362-23_2362-22insC
NM_025142.1:c.1918-23_1918-22insC NP_079418.1:n.1918-23_1918-22insC
XM_011525060.1:c.2362-23_2362-22insC XP_011523362.1:n.2362-23_2362-22insC
XM_011525060.2:c.2362-23_2362-22insC XP_011523362.1:n.2362-23_2362-22insC
NM_020791.4:c.2362-23_2362-22insC MANE Select NP_065842.1:n.2362-23_2362-22insC
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