Canonical Allele Identifier: CA2610296214

Gene: TCTN3

Linked Data

• gnomAD v4: 10-95686571-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95686576del , CM000672.2:g.95686576del	GRCh38
NC_000010.10:g.97446333del , CM000672.1:g.97446333del	GRCh37
NC_000010.9:g.97436323del	NCBI36
NG_032953.1:g.12572del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.853-42del MANE Select	ENSP00000360261.5:n.853-42del
ENST00000614499.5:c.907-42del	ENSP00000483364.2:n.907-42del
ENST00000679485.1:n.877-42del
ENST00000679566.1:c.852+472del	ENSP00000505964.1:n.852+472del
ENST00000679984.1:c.*108-42del	ENSP00000504998.1:n.*108-42del
ENST00000680144.1:c.853-42del	ENSP00000506398.1:n.853-42del
ENST00000680353.1:c.853-42del	ENSP00000505367.1:n.853-42del
ENST00000680697.1:n.543-1948del
ENST00000680709.1:c.616-42del	ENSP00000505830.1:n.616-42del
ENST00000681127.1:n.906-42del
ENST00000681739.1:n.908-42del
ENST00000681928.1:c.*130+472del	ENSP00000505552.1:n.*130+472del
ENST00000265993.13:c.907-42del	ENSP00000265993.9:n.907-42del
ENST00000371209.5:c.853-42del	ENSP00000360253.5:n.853-42del
ENST00000371217.9:c.853-42del	ENSP00000360261.5:n.853-42del
ENST00000430368.6:c.616-42del	ENSP00000387567.1:n.616-42del
ENST00000614499.4:c.853-42del	ENSP00000483364.1:n.853-42del
NM_001143973.1:c.616-42del	NP_001137445.1:n.616-42del
NM_015631.5:c.853-42del	NP_056446.4:n.853-42del
XM_005269690.1:c.907-42del	XP_005269747.1:n.907-42del
XM_011539627.1:c.907-42del	XP_011537929.1:n.907-42del
XM_011539628.1:c.907-42del	XP_011537930.1:n.907-42del
XM_005269690.2:c.907-42del	XP_005269747.1:n.907-42del
XM_011539627.2:c.907-42del	XP_011537929.1:n.907-42del
XM_011539628.2:c.907-42del	XP_011537930.1:n.907-42del
XM_024447935.1:c.907-42del	XP_024303703.1:n.907-42del
NM_015631.6:c.853-42del MANE Select	NP_056446.4:n.853-42del
NM_001143973.2:c.616-42del	NP_001137445.1:n.616-42del