Canonical Allele Identifier: CA211434428

Gene: TNKS2

Linked Data

• dbSNP Id: rs544591318
• gnomAD v2: 10-93587691-A-G
• gnomAD v3: 10-91827934-A-G
• gnomAD v4: 10-91827934-A-G
• MyVariant Identifiers: chr10:g.93587691A>G (hg19) ; chr10:g.91827934A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.91827934A>G , CM000672.2:g.91827934A>G	GRCh38
NC_000010.10:g.93587691A>G , CM000672.1:g.93587691A>G	GRCh37
NC_000010.9:g.93577671A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000710380.1:c.1022-351A>G	ENSP00000518237.1:n.1022-351A>G
ENST00000371627.5:c.983-351A>G MANE Select	ENSP00000360689.4:n.983-351A>G
ENST00000371627.4:c.983-351A>G	ENSP00000360689.4:n.983-351A>G
NM_025235.3:c.983-351A>G	NP_079511.1:n.983-351A>G
XM_011540213.1:c.1046-351A>G	XP_011538515.1:n.1046-351A>G
XM_011540214.1:c.407-351A>G	XP_011538516.1:n.407-351A>G
XM_005270185.4:c.1046-351A>G	XP_005270242.2:n.1046-351A>G
XM_017016696.1:c.983-351A>G	XP_016872185.1:n.983-351A>G
XM_017016697.1:c.662-351A>G	XP_016872186.1:n.662-351A>G
XM_017016698.2:c.662-351A>G	XP_016872187.1:n.662-351A>G
XM_017016699.1:c.662-351A>G	XP_016872188.1:n.662-351A>G
XM_017016700.2:c.407-351A>G	XP_016872189.1:n.407-351A>G
XM_017016701.1:c.1046-351A>G	XP_016872190.1:n.1046-351A>G
NM_025235.4:c.983-351A>G MANE Select	NP_079511.1:n.983-351A>G