Canonical Allele Identifier: CA398915001
Gene: TAOK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 871002
ClinVar RCV Id: RCV001090739
dbSNP Id: rs2032083321
MyVariant Identifiers: chr17:g.27857536A>G (hg19) chr17:g.29530518A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29530518A>G , CM000679.2:g.29530518A>G GRCh38
NC_000017.10:g.27857536A>G , CM000679.1:g.27857536A>G GRCh37
NC_000017.9:g.24881662A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261716.8:c.2260A>G MANE Select ENSP00000261716.3:p.Lys754Glu
ENST00000261716.7:c.2260A>G ENSP00000261716.3:p.Lys754Glu
ENST00000536202.1:c.1816A>G ENSP00000438819.1:p.Lys606Glu
ENST00000578653.1:n.344A>G
NM_020791.2:c.2260A>G NP_065842.1:p.Lys754Glu
NM_025142.1:c.1816A>G NP_079418.1:p.Lys606Glu
XM_011525060.1:c.2260A>G XP_011523362.1:p.Lys754Glu
XM_011525060.2:c.2260A>G XP_011523362.1:p.Lys754Glu
NM_020791.4:c.2260A>G MANE Select NP_065842.1:p.Lys754Glu
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