Canonical Allele Identifier: CA499151895

Gene: TAOK1

Linked Data

• dbSNP Id: rs1211613559
• gnomAD v2: 17-27860849-G-GAA
• gnomAD v3: 17-29533831-G-GAA
• gnomAD v4: 17-29533831-G-GAA
• MyVariant Identifiers: chr17:g.27860849_27860850insAA (hg19) ; chr17:g.29533831_29533832insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.29533831_29533832insAA , CM000679.2:g.29533831_29533832insAA	GRCh38
NC_000017.10:g.27860849_27860850insAA , CM000679.1:g.27860849_27860850insAA	GRCh37
NC_000017.9:g.24884975_24884976insAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261716.8:c.2362-287_2362-286insAA MANE Select	ENSP00000261716.3:n.2362-287_2362-286insAA
ENST00000261716.7:c.2362-287_2362-286insAA	ENSP00000261716.3:n.2362-287_2362-286insAA
ENST00000536202.1:c.1918-287_1918-286insAA	ENSP00000438819.1:n.1918-287_1918-286insAA
NM_020791.2:c.2362-287_2362-286insAA	NP_065842.1:n.2362-287_2362-286insAA
NM_025142.1:c.1918-287_1918-286insAA	NP_079418.1:n.1918-287_1918-286insAA
XM_011525060.1:c.2362-287_2362-286insAA	XP_011523362.1:n.2362-287_2362-286insAA
XM_011525060.2:c.2362-287_2362-286insAA	XP_011523362.1:n.2362-287_2362-286insAA
NM_020791.4:c.2362-287_2362-286insAA MANE Select	NP_065842.1:n.2362-287_2362-286insAA