Canonical Allele Identifier: CA2574645013

Gene: TWNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100988392_100988393del , CM000672.2:g.100988392_100988393del	GRCh38
NC_000010.10:g.102748149_102748150del , CM000672.1:g.102748149_102748150del	GRCh37
NC_000010.9:g.102738139_102738140del	NCBI36
NG_011646.1:g.4124_4125del
NG_012624.1:g.5857_5858del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.182_183del MANE Select	ENSP00000309595.2:p.Arg61ProfsTer?
ENST00000370228.2:c.182_183del	ENSP00000359248.1:p.Arg61ProfsTer?
ENST00000643860.1:c.182_183del	ENSP00000494389.1:p.Arg61ProfsTer?
ENST00000646226.1:n.58+779_58+780del
ENST00000311916.6:c.182_183del	ENSP00000309595.2:p.Arg61ProfsTer?
ENST00000370228.1:c.182_183del	ENSP00000359248.1:p.Arg61ProfsTer?
ENST00000459764.1:n.86+512_86+513del
ENST00000473656.5:n.64+779_64+780del
ENST00000476766.5:n.191+835_191+836del
NM_001163812.1:c.182_183del	NP_001157284.1:p.Arg61ProfsTer?
NM_001163813.1:c.-120+779_-120+780del	NP_001157285.1:n.-120+779_-120+780del
NM_001163814.1:c.-120+779_-120+780del	NP_001157286.1:n.-120+779_-120+780del
NM_021830.4:c.182_183del	NP_068602.2:p.Arg61ProfsTer?
XM_011539975.1:c.-58+779_-58+780del	XP_011538277.1:n.-58+779_-58+780del
XR_945788.1:n.1015_1016del
XM_011539975.2:c.-58+779_-58+780del	XP_011538277.1:n.-58+779_-58+780del
XM_017016437.1:c.-1119_-1118del	XP_016871926.1:n.-1119_-1118del
XR_001747142.1:n.356_357del
XR_001747144.1:n.356_357del
XR_002956991.1:n.356_357del
XR_945788.2:n.356_357del
NM_021830.5:c.182_183del MANE Select	NP_068602.2:p.Arg61ProfsTer?
NM_001163812.2:c.182_183del	NP_001157284.1:p.Arg61ProfsTer?
NM_001163813.2:c.-120+779_-120+780del	NP_001157285.1:n.-120+779_-120+780del
NM_001163814.2:c.-120+779_-120+780del	NP_001157286.1:n.-120+779_-120+780del
NM_001368275.1:c.-58+779_-58+780del	NP_001355204.1:n.-58+779_-58+780del
NR_160738.1:n.850_851del
NR_160739.1:n.71+779_71+780del
NR_160740.1:n.850_851del
NR_160741.1:n.850_851del
NR_160742.1:n.850_851del