Canonical Allele Identifier: CA595644175
Gene: TWNK HGNC NCBI

Linked Data

dbSNP Id: rs863223925

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100989863dup , CM000672.2:g.100989863dup GRCh38
NC_000010.10:g.102749620dup , CM000672.1:g.102749620dup GRCh37
NC_000010.9:g.102739610dup NCBI36
NG_011646.1:g.2655dup
NG_012624.1:g.7328dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000311916.8:c.1463dup MANE Select ENSP00000309595.2:p.His489ProfsTer21
ENST00000370228.2:c.1463dup ENSP00000359248.1:p.His489ProfsTer21
ENST00000643860.1:c.1463dup ENSP00000494389.1:p.His489ProfsTer21
ENST00000646226.1:n.278dup
ENST00000647109.1:c.122dup
ENST00000650396.1:c.424dup
ENST00000311916.6:c.1463dup ENSP00000309595.2:p.His489ProfsTer21
ENST00000370228.1:c.1463dup ENSP00000359248.1:p.His489ProfsTer21
ENST00000459764.1:n.306dup
ENST00000473656.5:n.284dup
ENST00000476766.5:n.349dup
NM_001163812.1:c.1463dup NP_001157284.1:p.His489ProfsTer21
NM_001163813.1:c.101dup NP_001157285.1:p.His35ProfsTer21
NM_001163814.1:c.101dup NP_001157286.1:p.His35ProfsTer21
NM_021830.4:c.1463dup NP_068602.2:p.His489ProfsTer21
XM_011539974.1:c.101dup XP_011538276.1:p.His35ProfsTer21
XM_011539975.1:c.101dup XP_011538277.1:p.His35ProfsTer21
XR_945788.1:n.2234dup
XM_011539975.2:c.101dup XP_011538277.1:p.His35ProfsTer21
XM_017016437.1:c.101dup XP_016871926.1:p.His35ProfsTer21
XR_001747142.1:n.1637dup
XR_001747144.1:n.1575dup
XR_002956991.1:n.1575dup
XR_945788.2:n.1575dup
NM_021830.5:c.1463dup MANE Select NP_068602.2:p.His489ProfsTer21
NM_001163812.2:c.1463dup NP_001157284.1:p.His489ProfsTer21
NM_001163813.2:c.101dup NP_001157285.1:p.His35ProfsTer21
NM_001163814.2:c.101dup NP_001157286.1:p.His35ProfsTer21
NM_001368275.1:c.101dup NP_001355204.1:p.His35ProfsTer21
NR_160738.1:n.2131dup
NR_160739.1:n.291dup
NR_160740.1:n.2069dup
NR_160741.1:n.2069dup
NR_160742.1:n.2069dup