Canonical Allele Identifier: CA8474838
Gene: TAOK1 HGNC NCBI

Linked Data

dbSNP Id: rs763177640
ExAC: 17:27861104 CTT / C
gnomAD v2: 17-27861104-CTT-C
gnomAD v3: 17-29534086-CTT-C
gnomAD v4: 17-29534086-CTT-C
MyVariant Identifiers: chr17:g.27861105_27861106del (hg19) chr17:g.29534087_29534088del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29534095_29534096del , CM000679.2:g.29534095_29534096del GRCh38
NC_000017.10:g.27861113_27861114del , CM000679.1:g.27861113_27861114del GRCh37
NC_000017.9:g.24885239_24885240del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261716.8:c.2362-23_2362-22del MANE Select ENSP00000261716.3:n.2362-23_2362-22del
ENST00000261716.7:c.2362-23_2362-22del ENSP00000261716.3:n.2362-23_2362-22del
ENST00000536202.1:c.1918-23_1918-22del ENSP00000438819.1:n.1918-23_1918-22del
NM_020791.2:c.2362-23_2362-22del NP_065842.1:n.2362-23_2362-22del
NM_025142.1:c.1918-23_1918-22del NP_079418.1:n.1918-23_1918-22del
XM_011525060.1:c.2362-23_2362-22del XP_011523362.1:n.2362-23_2362-22del
XM_011525060.2:c.2362-23_2362-22del XP_011523362.1:n.2362-23_2362-22del
NM_020791.4:c.2362-23_2362-22del MANE Select NP_065842.1:n.2362-23_2362-22del
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