Canonical Allele Identifier: CA13272316
Gene: TNKS2 HGNC NCBI

Linked Data

dbSNP Id: rs10509637

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.91827975A>G , CM000672.2:g.91827975A>G GRCh38
NC_000010.10:g.93587732A>G , CM000672.1:g.93587732A>G GRCh37
NC_000010.9:g.93577712A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000710380.1:c.1022-310A>G ENSP00000518237.1:n.1022-310A>G
ENST00000371627.5:c.983-310A>G MANE Select ENSP00000360689.4:n.983-310A>G
ENST00000371627.4:c.983-310A>G ENSP00000360689.4:n.983-310A>G
NM_025235.3:c.983-310A>G NP_079511.1:n.983-310A>G
XM_011540213.1:c.1046-310A>G XP_011538515.1:n.1046-310A>G
XM_011540214.1:c.407-310A>G XP_011538516.1:n.407-310A>G
XM_005270185.4:c.1046-310A>G XP_005270242.2:n.1046-310A>G
XM_017016696.1:c.983-310A>G XP_016872185.1:n.983-310A>G
XM_017016697.1:c.662-310A>G XP_016872186.1:n.662-310A>G
XM_017016698.2:c.662-310A>G XP_016872187.1:n.662-310A>G
XM_017016699.1:c.662-310A>G XP_016872188.1:n.662-310A>G
XM_017016700.2:c.407-310A>G XP_016872189.1:n.407-310A>G
XM_017016701.1:c.1046-310A>G XP_016872190.1:n.1046-310A>G
NM_025235.4:c.983-310A>G MANE Select NP_079511.1:n.983-310A>G