Canonical Allele Identifier: CA2254771468
Gene: TAOK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29451917_29451919delinsAAG , CM000679.2:g.29451917_29451919delinsAAG GRCh38
NC_000017.10:g.27778935_27778937delinsAAG , CM000679.1:g.27778935_27778937delinsAAG GRCh37
NC_000017.9:g.24803061_24803063delinsAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261716.8:c.132+237_132+239delinsAAG MANE Select ENSP00000261716.3:n.132+237_132+239delinsAAG
ENST00000261716.7:c.132+237_132+239delinsAAG ENSP00000261716.3:n.132+237_132+239delinsAAG
ENST00000536202.1:c.132+237_132+239delinsAAG ENSP00000438819.1:n.132+237_132+239delinsAAG
ENST00000583121.5:c.132+237_132+239delinsAAG ENSP00000464562.1:n.132+237_132+239delinsAAG
NM_020791.2:c.132+237_132+239delinsAAG NP_065842.1:n.132+237_132+239delinsAAG
NM_025142.1:c.132+237_132+239delinsAAG NP_079418.1:n.132+237_132+239delinsAAG
XM_011525060.1:c.132+237_132+239delinsAAG XP_011523362.1:n.132+237_132+239delinsAAG
XM_011525060.2:c.132+237_132+239delinsAAG XP_011523362.1:n.132+237_132+239delinsAAG
NM_020791.4:c.132+237_132+239delinsAAG MANE Select NP_065842.1:n.132+237_132+239delinsAAG