Canonical Allele Identifier: CA1927901326
Gene: TNKS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.91827894C= , CM000672.2:g.91827894C= GRCh38
NC_000010.10:g.93587651C= , CM000672.1:g.93587651C= GRCh37
NC_000010.9:g.93577631C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000710380.1:c.1022-391C= ENSP00000518237.1:n.1022-391C=
ENST00000371627.5:c.983-391C= MANE Select ENSP00000360689.4:n.983-391C=
ENST00000371627.4:c.983-391C= ENSP00000360689.4:n.983-391C=
NM_025235.3:c.983-391C= NP_079511.1:n.983-391C=
XM_011540213.1:c.1046-391C= XP_011538515.1:n.1046-391C=
XM_011540214.1:c.407-391C= XP_011538516.1:n.407-391C=
XM_005270185.4:c.1046-391C= XP_005270242.2:n.1046-391C=
XM_017016696.1:c.983-391C= XP_016872185.1:n.983-391C=
XM_017016697.1:c.662-391C= XP_016872186.1:n.662-391C=
XM_017016698.2:c.662-391C= XP_016872187.1:n.662-391C=
XM_017016699.1:c.662-391C= XP_016872188.1:n.662-391C=
XM_017016700.2:c.407-391C= XP_016872189.1:n.407-391C=
XM_017016701.1:c.1046-391C= XP_016872190.1:n.1046-391C=
NM_025235.4:c.983-391C= MANE Select NP_079511.1:n.983-391C=