Canonical Allele Identifier: CA727879491

Gene: TAOK1

Linked Data

• dbSNP Id: rs1300763621
• gnomAD v4: 17-29510819-TTATC-T
• MyVariant Identifiers: chr17:g.27837838_27837841del (hg19) ; chr17:g.29510820_29510823del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.29510822_29510825del , CM000679.2:g.29510822_29510825del	GRCh38
NC_000017.10:g.27837840_27837843del , CM000679.1:g.27837840_27837843del	GRCh37
NC_000017.9:g.24861966_24861969del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261716.8:c.1576-42_1576-39del MANE Select	ENSP00000261716.3:n.1576-42_1576-39del
ENST00000261716.7:c.1576-42_1576-39del	ENSP00000261716.3:n.1576-42_1576-39del
ENST00000536202.1:c.1576-42_1576-39del	ENSP00000438819.1:n.1576-42_1576-39del
ENST00000577583.1:n.1424-42_1424-39del
NM_020791.2:c.1576-42_1576-39del	NP_065842.1:n.1576-42_1576-39del
NM_025142.1:c.1576-42_1576-39del	NP_079418.1:n.1576-42_1576-39del
XM_011525060.1:c.1576-42_1576-39del	XP_011523362.1:n.1576-42_1576-39del
XM_011525060.2:c.1576-42_1576-39del	XP_011523362.1:n.1576-42_1576-39del
NM_020791.4:c.1576-42_1576-39del MANE Select	NP_065842.1:n.1576-42_1576-39del