Canonical Allele Identifier: CA595639358
Gene: TCTN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95664072_95664073del , CM000672.2:g.95664072_95664073del GRCh38
NC_000010.10:g.97423829_97423830del , CM000672.1:g.97423829_97423830del GRCh37
NC_000010.9:g.97413819_97413820del NCBI36
NG_032953.1:g.35072_35073del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371217.10:c.1819_1820del MANE Select ENSP00000360261.5:p.Met607ValfsTer6
ENST00000614499.5:c.1858_1859del ENSP00000483364.2:p.Met620ValfsTer6
ENST00000679984.1:c.*1059_*1060del ENSP00000504998.1:n.*1059_*1060del
ENST00000680144.1:c.1723_1724del ENSP00000506398.1:p.Met575ValfsTer6
ENST00000680353.1:c.1570_1571del ENSP00000505367.1:p.Met524ValfsTer6
ENST00000680697.1:n.2014_2015del
ENST00000680709.1:c.1567_1568del ENSP00000505830.1:p.Met523ValfsTer6
ENST00000680781.1:c.476_477del
ENST00000681185.1:n.521_522del
ENST00000681739.1:n.2200_2201del
ENST00000681928.1:c.*359_*360del ENSP00000505552.1:n.*359_*360del
ENST00000265993.13:c.1873_1874del ENSP00000265993.9:p.Met625ValfsTer6
ENST00000371217.9:c.1819_1820del ENSP00000360261.5:p.Met607ValfsTer6
ENST00000430368.6:c.1375_1376del ENSP00000387567.1:p.Met459ValfsTer6
ENST00000614499.4:c.1819_1820del ENSP00000483364.1:p.Met607ValfsTer6
NM_001143973.1:c.1375_1376del NP_001137445.1:p.Met459ValfsTer6
NM_015631.5:c.1819_1820del NP_056446.4:p.Met607ValfsTer6
XM_005269690.1:c.1792_1793del XP_005269747.1:p.Met598ValfsTer6
XM_011539627.1:c.1858_1859del XP_011537929.1:p.Met620ValfsTer6
XM_011539628.1:c.1735_1736del XP_011537930.1:p.Met579ValfsTer6
XM_005269690.2:c.1792_1793del XP_005269747.1:p.Met598ValfsTer6
XM_011539627.2:c.1858_1859del XP_011537929.1:p.Met620ValfsTer6
XM_011539628.2:c.1735_1736del XP_011537930.1:p.Met579ValfsTer6
XM_024447935.1:c.1777_1778del XP_024303703.1:p.Met593ValfsTer6
NM_015631.6:c.1819_1820del MANE Select NP_056446.4:p.Met607ValfsTer6
NM_001143973.2:c.1375_1376del NP_001137445.1:p.Met459ValfsTer6