Canonical Allele Identifier: CA2254780603
Gene: TAOK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29477856_29477861delinsGCTGTC , CM000679.2:g.29477856_29477861delinsGCTGTC GRCh38
NC_000017.10:g.27804874_27804879delinsGCTGTC , CM000679.1:g.27804874_27804879delinsGCTGTC GRCh37
NC_000017.9:g.24829000_24829005delinsGCTGTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261716.8:c.352+150_352+155delinsGCTGTC MANE Select ENSP00000261716.3:n.352+150_352+155delinsGCTGTC
ENST00000261716.7:c.352+150_352+155delinsGCTGTC ENSP00000261716.3:n.352+150_352+155delinsGCTGTC
ENST00000536202.1:c.352+150_352+155delinsGCTGTC ENSP00000438819.1:n.352+150_352+155delinsGCTGTC
NM_020791.2:c.352+150_352+155delinsGCTGTC NP_065842.1:n.352+150_352+155delinsGCTGTC
NM_025142.1:c.352+150_352+155delinsGCTGTC NP_079418.1:n.352+150_352+155delinsGCTGTC
XM_011525060.1:c.352+150_352+155delinsGCTGTC XP_011523362.1:n.352+150_352+155delinsGCTGTC
XM_011525060.2:c.352+150_352+155delinsGCTGTC XP_011523362.1:n.352+150_352+155delinsGCTGTC
NM_020791.4:c.352+150_352+155delinsGCTGTC MANE Select NP_065842.1:n.352+150_352+155delinsGCTGTC