Canonical Allele Identifier: CA828564709

Gene: TTK

Linked Data

• dbSNP Id: rs1404016943
• gnomAD v4: 6-80037906-A-G
• MyVariant Identifiers: chr6:g.80747623A>G (hg19) ; chr6:g.80037906A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80037906A>G , CM000668.2:g.80037906A>G	GRCh38
NC_000006.11:g.80747623A>G , CM000668.1:g.80747623A>G	GRCh37
NC_000006.10:g.80804342A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369798.7:c.2050-61A>G MANE Select	ENSP00000358813.2:n.2050-61A>G
ENST00000230510.7:c.2047-61A>G	ENSP00000230510.3:n.2047-61A>G
ENST00000369798.6:c.2050-61A>G	ENSP00000358813.2:n.2050-61A>G
ENST00000504590.1:n.354A>G
ENST00000509894.5:c.2047-61A>G	ENSP00000422936.1:n.2047-61A>G
NM_001166691.1:c.2047-61A>G	NP_001160163.1:n.2047-61A>G
NM_003318.4:c.2050-61A>G	NP_003309.2:n.2050-61A>G
XM_011536099.1:c.2050-61A>G	XP_011534401.1:n.2050-61A>G
XM_011536100.1:c.2047-61A>G	XP_011534402.1:n.2047-61A>G
XM_011536099.3:c.2050-61A>G	XP_011534401.1:n.2050-61A>G
XM_011536100.3:c.2047-61A>G	XP_011534402.1:n.2047-61A>G
XM_017011242.2:c.1885-61A>G	XP_016866731.1:n.1885-61A>G
NM_003318.5:c.2050-61A>G MANE Select	NP_003309.2:n.2050-61A>G
NM_001166691.2:c.2047-61A>G	NP_001160163.1:n.2047-61A>G