Canonical Allele Identifier: CA915947586
Community Standard Title: NM_021830.5(TWNK):c.49del (p.Leu17CysfsTer?)
Gene: TWNK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100988259del , CM000672.2:g.100988259del GRCh38
NC_000010.10:g.102748016del , CM000672.1:g.102748016del GRCh37
NC_000010.9:g.102738006del NCBI36
NG_011646.1:g.4260del
NG_012624.1:g.5724del

Transcript Alleles

HGVS Amino-acid Change
NM_021830.5:c.49del MANE Select NP_068602.2:p.Leu17CysfsTer?
ENST00000311916.8:c.49del MANE Select ENSP00000309595.2:p.Leu17CysfsTer?
NM_001163812.1:c.49del NP_001157284.1:p.Leu17CysfsTer?
NM_001163812.2:c.49del NP_001157284.1:p.Leu17CysfsTer?
NM_001163813.1:c.-120+646del NP_001157285.1:n.-120+646del
NM_001163813.2:c.-120+646del NP_001157285.1:n.-120+646del
NM_001163814.1:c.-120+646del NP_001157286.1:n.-120+646del
NM_001163814.2:c.-120+646del NP_001157286.1:n.-120+646del
NM_001368275.1:c.-58+646del NP_001355204.1:n.-58+646del
NM_021830.4:c.49del NP_068602.2:p.Leu17CysfsTer?
NR_160738.1:n.717del
NR_160739.1:n.71+646del
NR_160740.1:n.717del
NR_160741.1:n.717del
NR_160742.1:n.717del
ENST00000311916.6:c.49del ENSP00000309595.2:p.Leu17CysfsTer?
ENST00000370228.1:c.49del ENSP00000359248.1:p.Leu17CysfsTer?
ENST00000370228.2:c.49del ENSP00000359248.1:p.Leu17CysfsTer?
ENST00000459764.1:n.86+379del
ENST00000473656.5:n.64+646del
ENST00000476766.5:n.191+702del
ENST00000643860.1:c.49del ENSP00000494389.1:p.Leu17CysfsTer?
ENST00000646226.1:n.58+646del
XM_011539975.1:c.-58+646del XP_011538277.1:n.-58+646del
XM_011539975.2:c.-58+646del XP_011538277.1:n.-58+646del
XM_017016437.1:c.-1252del XP_016871926.1:n.-1252del
XR_001747142.1:n.223del
XR_001747144.1:n.223del
XR_002956991.1:n.223del
XR_945788.1:n.882del
XR_945788.2:n.223del