Canonical Allele Identifier: CA4620749

Gene: TNKS

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.9679917A>C , CM000670.2:g.9679917A>C	GRCh38
NC_000008.10:g.9537427A>C , CM000670.1:g.9537427A>C	GRCh37
NC_000008.9:g.9574837A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517770.2:c.995-34A>C	ENSP00000428185.2:n.995-34A>C
ENST00000310430.11:c.995-34A>C MANE Select	ENSP00000311579.6:n.995-34A>C
ENST00000310430.10:c.995-34A>C	ENSP00000311579.6:n.995-34A>C
ENST00000517989.1:n.72A>C
ENST00000518027.5:n.294-34A>C
ENST00000518281.5:c.284-34A>C	ENSP00000429890.1:n.284-34A>C
ENST00000519392.5:n.84-34A>C
ENST00000520408.5:c.995-34A>C	ENSP00000428299.1:n.995-34A>C
ENST00000521039.5:n.277-34A>C
NM_003747.2:c.995-34A>C	NP_003738.2:n.995-34A>C
XM_006716263.2:c.995-34A>C	XP_006716326.1:n.995-34A>C
XM_011543845.1:c.995-34A>C	XP_011542147.1:n.995-34A>C
XM_011543846.1:c.995-34A>C	XP_011542148.1:n.995-34A>C
XM_011543847.1:c.995-34A>C	XP_011542149.1:n.995-34A>C
XM_006716263.4:c.995-34A>C	XP_006716326.1:n.995-34A>C
XM_011543845.3:c.995-34A>C	XP_011542147.1:n.995-34A>C
XM_011543846.3:c.995-34A>C	XP_011542148.1:n.995-34A>C
NM_003747.3:c.995-34A>C MANE Select	NP_003738.2:n.995-34A>C