Canonical Allele Identifier: CA1762816887

Gene: TNKS

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.9744189G>A , CM000670.2:g.9744189G>A	GRCh38
NC_000008.10:g.9601699G>A , CM000670.1:g.9601699G>A	GRCh37
NC_000008.9:g.9639109G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517770.2:c.2644-3835G>A	ENSP00000428185.2:n.2644-3835G>A
ENST00000518635.2:c.313+617G>A	ENSP00000431098.1:n.313+617G>A
ENST00000310430.11:c.2644-3835G>A MANE Select	ENSP00000311579.6:n.2644-3835G>A
ENST00000310430.10:c.2644-3835G>A	ENSP00000311579.6:n.2644-3835G>A
ENST00000518281.5:c.1933-3835G>A	ENSP00000429890.1:n.1933-3835G>A
ENST00000518635.1:c.313+617G>A	ENSP00000431098.1:n.313+617G>A
ENST00000519191.1:n.202+3074G>A
NM_003747.2:c.2644-3835G>A	NP_003738.2:n.2644-3835G>A
XM_006716263.2:c.2644-3835G>A	XP_006716326.1:n.2644-3835G>A
XM_011543845.1:c.2644-3835G>A	XP_011542147.1:n.2644-3835G>A
XM_011543846.1:c.2644-3835G>A	XP_011542148.1:n.2644-3835G>A
XM_011543847.1:c.2332-3835G>A	XP_011542149.1:n.2332-3835G>A
XM_006716263.4:c.2644-3835G>A	XP_006716326.1:n.2644-3835G>A
XM_011543845.3:c.2644-3835G>A	XP_011542147.1:n.2644-3835G>A
XM_011543846.3:c.2644-3835G>A	XP_011542148.1:n.2644-3835G>A
NM_003747.3:c.2644-3835G>A MANE Select	NP_003738.2:n.2644-3835G>A