Canonical Allele Identifier: CA3902281

Gene: TTK

Linked Data

• dbSNP Id: rs764752440
• ExAC: 6:80747633 G / A
• gnomAD v2: 6-80747633-G-A
• gnomAD v4: 6-80037916-G-A
• MyVariant Identifiers: chr6:g.80747633G>A (hg19) ; chr6:g.80037916G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80037916G>A , CM000668.2:g.80037916G>A	GRCh38
NC_000006.11:g.80747633G>A , CM000668.1:g.80747633G>A	GRCh37
NC_000006.10:g.80804352G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369798.7:c.2050-51G>A MANE Select	ENSP00000358813.2:n.2050-51G>A
ENST00000230510.7:c.2047-51G>A	ENSP00000230510.3:n.2047-51G>A
ENST00000369798.6:c.2050-51G>A	ENSP00000358813.2:n.2050-51G>A
ENST00000504590.1:n.364G>A
ENST00000509894.5:c.2047-51G>A	ENSP00000422936.1:n.2047-51G>A
NM_001166691.1:c.2047-51G>A	NP_001160163.1:n.2047-51G>A
NM_003318.4:c.2050-51G>A	NP_003309.2:n.2050-51G>A
XM_011536099.1:c.2050-51G>A	XP_011534401.1:n.2050-51G>A
XM_011536100.1:c.2047-51G>A	XP_011534402.1:n.2047-51G>A
XM_011536099.3:c.2050-51G>A	XP_011534401.1:n.2050-51G>A
XM_011536100.3:c.2047-51G>A	XP_011534402.1:n.2047-51G>A
XM_017011242.2:c.1885-51G>A	XP_016866731.1:n.1885-51G>A
NM_003318.5:c.2050-51G>A MANE Select	NP_003309.2:n.2050-51G>A
NM_001166691.2:c.2047-51G>A	NP_001160163.1:n.2047-51G>A