Canonical Allele Identifier: CA2254771469
Gene: TAOK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29451918_29451922delinsAGAAT , CM000679.2:g.29451918_29451922delinsAGAAT GRCh38
NC_000017.10:g.27778936_27778940delinsAGAAT , CM000679.1:g.27778936_27778940delinsAGAAT GRCh37
NC_000017.9:g.24803062_24803066delinsAGAAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261716.8:c.132+238_132+242delinsAGAAT MANE Select ENSP00000261716.3:n.132+238_132+242delinsAGAAT
ENST00000261716.7:c.132+238_132+242delinsAGAAT ENSP00000261716.3:n.132+238_132+242delinsAGAAT
ENST00000536202.1:c.132+238_132+242delinsAGAAT ENSP00000438819.1:n.132+238_132+242delinsAGAAT
ENST00000583121.5:c.132+238_132+242delinsAGAAT ENSP00000464562.1:n.132+238_132+242delinsAGAAT
NM_020791.2:c.132+238_132+242delinsAGAAT NP_065842.1:n.132+238_132+242delinsAGAAT
NM_025142.1:c.132+238_132+242delinsAGAAT NP_079418.1:n.132+238_132+242delinsAGAAT
XM_011525060.1:c.132+238_132+242delinsAGAAT XP_011523362.1:n.132+238_132+242delinsAGAAT
XM_011525060.2:c.132+238_132+242delinsAGAAT XP_011523362.1:n.132+238_132+242delinsAGAAT
NM_020791.4:c.132+238_132+242delinsAGAAT MANE Select NP_065842.1:n.132+238_132+242delinsAGAAT
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