Canonical Allele Identifier: CA727879436
Gene: TAOK1 HGNC NCBI

Linked Data

dbSNP Id: rs1482378505
gnomAD v3: 17-29510714-CAT-C
gnomAD v4: 17-29510714-CAT-C
MyVariant Identifiers: chr17:g.27837733_27837734del (hg19) chr17:g.29510715_29510716del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29510715_29510716del , CM000679.2:g.29510715_29510716del GRCh38
NC_000017.10:g.27837733_27837734del , CM000679.1:g.27837733_27837734del GRCh37
NC_000017.9:g.24861859_24861860del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261716.8:c.1576-149_1576-148del MANE Select ENSP00000261716.3:n.1576-149_1576-148del
ENST00000261716.7:c.1576-149_1576-148del ENSP00000261716.3:n.1576-149_1576-148del
ENST00000536202.1:c.1576-149_1576-148del ENSP00000438819.1:n.1576-149_1576-148del
ENST00000577583.1:n.1424-149_1424-148del
NM_020791.2:c.1576-149_1576-148del NP_065842.1:n.1576-149_1576-148del
NM_025142.1:c.1576-149_1576-148del NP_079418.1:n.1576-149_1576-148del
XM_011525060.1:c.1576-149_1576-148del XP_011523362.1:n.1576-149_1576-148del
XM_011525060.2:c.1576-149_1576-148del XP_011523362.1:n.1576-149_1576-148del
NM_020791.4:c.1576-149_1576-148del MANE Select NP_065842.1:n.1576-149_1576-148del
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