Canonical Allele Identifier: CA279556
Gene: TCTN2 HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.123704545del , CM000674.2:g.123704545del GRCh38
NC_000012.11:g.124189092del , CM000674.1:g.124189092del GRCh37
NC_000012.10:g.122755045del NCBI36
NG_030442.1:g.38433del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303372.7:c.1626del MANE Select ENSP00000304941.5:p.Asp543IlefsTer11
ENST00000679504.1:c.1623del ENSP00000505006.1:p.Asp542IlefsTer11
ENST00000680394.1:n.727del
ENST00000680500.1:c.1744del ENSP00000506438.1:p.Ter582AspextTer?
ENST00000680574.1:c.1491del ENSP00000505356.1:p.Asp498IlefsTer11
ENST00000303372.6:c.1626del ENSP00000304941.5:p.Asp543IlefsTer11
ENST00000426174.6:c.1623del ENSP00000395171.2:p.Asp542IlefsTer11
ENST00000543998.1:n.2398del
NM_001143850.2:c.1623del NP_001137322.1:p.Asp542IlefsTer11
NM_024809.4:c.1626del NP_079085.2:p.Asp543IlefsTer11
XM_005253623.2:c.1491del XP_005253680.1:p.Asp498IlefsTer11
XM_006719605.2:c.1626del XP_006719668.1:p.Asp543IlefsTer11
XM_011538748.1:c.714del XP_011537050.1:p.Asp239IlefsTer11
XM_006719605.3:c.1626del XP_006719668.1:p.Asp543IlefsTer11
XM_017019974.1:c.1488del XP_016875463.1:p.Asp497IlefsTer11
XM_017019975.1:c.714del XP_016875464.1:p.Asp239IlefsTer11
NM_024809.5:c.1626del MANE Select NP_079085.2:p.Asp543IlefsTer11
NM_001143850.3:c.1623del NP_001137322.1:p.Asp542IlefsTer11