Canonical Allele Identifier: CA2518016811
Gene: TAOK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29510972_29510973insAAATGTCAATGGTCACTGAA , CM000679.2:g.29510972_29510973insAAATGTCAATGGTCACTGAA GRCh38
NC_000017.10:g.27837990_27837991insAAATGTCAATGGTCACTGAA , CM000679.1:g.27837990_27837991insAAATGTCAATGGTCACTGAA GRCh37
NC_000017.9:g.24862116_24862117insAAATGTCAATGGTCACTGAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261716.8:c.1684_1685insAAATGTCAATGGTCACTGAA MANE Select ENSP00000261716.3:p.Arg562GlnfsTer16
ENST00000261716.7:c.1684_1685insAAATGTCAATGGTCACTGAA ENSP00000261716.3:p.Arg562GlnfsTer16
ENST00000536202.1:c.1684_1685insAAATGTCAATGGTCACTGAA ENSP00000438819.1:p.Arg562GlnfsTer20
ENST00000577583.1:n.1532_1533insAAATGTCAATGGTCACTGAA
NM_020791.2:c.1684_1685insAAATGTCAATGGTCACTGAA NP_065842.1:p.Arg562GlnfsTer16
NM_025142.1:c.1684_1685insAAATGTCAATGGTCACTGAA NP_079418.1:p.Arg562GlnfsTer20
XM_011525060.1:c.1684_1685insAAATGTCAATGGTCACTGAA XP_011523362.1:p.Arg562GlnfsTer16
XM_011525060.2:c.1684_1685insAAATGTCAATGGTCACTGAA XP_011523362.1:p.Arg562GlnfsTer16
NM_020791.4:c.1684_1685insAAATGTCAATGGTCACTGAA MANE Select NP_065842.1:p.Arg562GlnfsTer16