Canonical Allele Identifier: CA5621045
Gene: TCTN3 HGNC NCBI

Linked Data

dbSNP Id: rs749742779

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95686570C>T , CM000672.2:g.95686570C>T GRCh38
NC_000010.10:g.97446327C>T , CM000672.1:g.97446327C>T GRCh37
NC_000010.9:g.97436317C>T NCBI36
NG_032953.1:g.12574G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371217.10:c.853-40G>A MANE Select ENSP00000360261.5:n.853-40G>A
ENST00000614499.5:c.907-40G>A ENSP00000483364.2:n.907-40G>A
ENST00000679485.1:n.877-40G>A
ENST00000679566.1:c.852+474G>A ENSP00000505964.1:n.852+474G>A
ENST00000679984.1:c.*108-40G>A ENSP00000504998.1:n.*108-40G>A
ENST00000680144.1:c.853-40G>A ENSP00000506398.1:n.853-40G>A
ENST00000680353.1:c.853-40G>A ENSP00000505367.1:n.853-40G>A
ENST00000680697.1:n.543-1946G>A
ENST00000680709.1:c.616-40G>A ENSP00000505830.1:n.616-40G>A
ENST00000681127.1:n.906-40G>A
ENST00000681739.1:n.908-40G>A
ENST00000681928.1:c.*130+474G>A ENSP00000505552.1:n.*130+474G>A
ENST00000265993.13:c.907-40G>A ENSP00000265993.9:n.907-40G>A
ENST00000371209.5:c.853-40G>A ENSP00000360253.5:n.853-40G>A
ENST00000371217.9:c.853-40G>A ENSP00000360261.5:n.853-40G>A
ENST00000430368.6:c.616-40G>A ENSP00000387567.1:n.616-40G>A
ENST00000614499.4:c.853-40G>A ENSP00000483364.1:n.853-40G>A
NM_001143973.1:c.616-40G>A NP_001137445.1:n.616-40G>A
NM_015631.5:c.853-40G>A NP_056446.4:n.853-40G>A
XM_005269690.1:c.907-40G>A XP_005269747.1:n.907-40G>A
XM_011539627.1:c.907-40G>A XP_011537929.1:n.907-40G>A
XM_011539628.1:c.907-40G>A XP_011537930.1:n.907-40G>A
XM_005269690.2:c.907-40G>A XP_005269747.1:n.907-40G>A
XM_011539627.2:c.907-40G>A XP_011537929.1:n.907-40G>A
XM_011539628.2:c.907-40G>A XP_011537930.1:n.907-40G>A
XM_024447935.1:c.907-40G>A XP_024303703.1:n.907-40G>A
NM_015631.6:c.853-40G>A MANE Select NP_056446.4:n.853-40G>A
NM_001143973.2:c.616-40G>A NP_001137445.1:n.616-40G>A