Canonical Allele Identifier: CA669867137

Gene: TNKS2

Linked Data

• dbSNP Id: rs1158424792
• gnomAD v3: 10-91827923-C-A
• gnomAD v4: 10-91827923-C-A
• MyVariant Identifiers: chr10:g.93587680C>A (hg19) ; chr10:g.91827923C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.91827923C>A , CM000672.2:g.91827923C>A	GRCh38
NC_000010.10:g.93587680C>A , CM000672.1:g.93587680C>A	GRCh37
NC_000010.9:g.93577660C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000710380.1:c.1022-362C>A	ENSP00000518237.1:n.1022-362C>A
ENST00000371627.5:c.983-362C>A MANE Select	ENSP00000360689.4:n.983-362C>A
ENST00000371627.4:c.983-362C>A	ENSP00000360689.4:n.983-362C>A
NM_025235.3:c.983-362C>A	NP_079511.1:n.983-362C>A
XM_011540213.1:c.1046-362C>A	XP_011538515.1:n.1046-362C>A
XM_011540214.1:c.407-362C>A	XP_011538516.1:n.407-362C>A
XM_005270185.4:c.1046-362C>A	XP_005270242.2:n.1046-362C>A
XM_017016696.1:c.983-362C>A	XP_016872185.1:n.983-362C>A
XM_017016697.1:c.662-362C>A	XP_016872186.1:n.662-362C>A
XM_017016698.2:c.662-362C>A	XP_016872187.1:n.662-362C>A
XM_017016699.1:c.662-362C>A	XP_016872188.1:n.662-362C>A
XM_017016700.2:c.407-362C>A	XP_016872189.1:n.407-362C>A
XM_017016701.1:c.1046-362C>A	XP_016872190.1:n.1046-362C>A
NM_025235.4:c.983-362C>A MANE Select	NP_079511.1:n.983-362C>A