Canonical Allele Identifier: CA12828680
Gene: TNKS HGNC NCBI
gnomAD v4:

Genomic Alleles

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

Transcript Alleles

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