Canonical Allele Identifier: CA398917377
Gene: TAOK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1309471
ClinVar RCV Id: RCV001765640
dbSNP Id: rs2150774822
MyVariant Identifiers: chr17:g.27861277G>T (hg19) chr17:g.29534259G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29534259G>T , CM000679.2:g.29534259G>T GRCh38
NC_000017.10:g.27861277G>T , CM000679.1:g.27861277G>T GRCh37
NC_000017.9:g.24885403G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261716.8:c.2503G>T MANE Select ENSP00000261716.3:p.Glu835Ter
ENST00000261716.7:c.2503G>T ENSP00000261716.3:p.Glu835Ter
ENST00000536202.1:c.2059G>T ENSP00000438819.1:p.Glu687Ter
NM_020791.2:c.2503G>T NP_065842.1:p.Glu835Ter
NM_025142.1:c.2059G>T NP_079418.1:p.Glu687Ter
XM_011525060.1:c.2503G>T XP_011523362.1:p.Glu835Ter
XM_011525060.2:c.2503G>T XP_011523362.1:p.Glu835Ter
NM_020791.4:c.2503G>T MANE Select NP_065842.1:p.Glu835Ter
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