Canonical Allele Identifier: CA277376

Linked Data

ClinVar Variation Id: 212386
ClinVar RCV Id: RCV000194752
dbSNP Id: rs797046039

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110636502del , CM000674.2:g.110636502del GRCh38
NC_000012.11:g.111074307del , CM000674.1:g.111074307del GRCh37
NC_000012.10:g.109558690del NCBI36
NG_030381.1:g.27476del

Transcript Alleles

HGVS Amino-acid change
ENST00000377654.5:c.843+1del (TCTN1)
ENST00000397659.9:c.843+1del (TCTN1)
ENST00000471804.7:c.843+1del (TCTN1)
ENST00000547461.3:c.*13+1del (TCTN1)
ENST00000549123.6:c.843+1del (TCTN1)
ENST00000552038.6:n.913+1del (TCTN1)
ENST00000614115.5:c.843+1del (TCTN1)
ENST00000679473.1:c.*476+1del (TCTN1)
ENST00000679617.1:c.*455+1del (TCTN1)
ENST00000679713.1:c.*476+1del (TCTN1)
ENST00000680068.1:c.*557+1del (TCTN1)
ENST00000680168.1:n.490+1del (TCTN1)
ENST00000680445.1:c.843+1del (TCTN1)
ENST00000680512.1:c.*345+1del (TCTN1)
ENST00000681395.1:c.*345+1del (TCTN1)
ENST00000681604.1:c.*667+1del (TCTN1)
ENST00000681807.1:c.*557+1del (TCTN1)
ENST00000681851.1:c.*132+1del (TCTN1)
ENST00000377654.4:c.663+1del (TCTN1)
ENST00000397655.7:c.801+1del (TCTN1)
ENST00000397656.8:c.*476+1del (TCTN1)
ENST00000397659.8:c.843+1del (TCTN1)
ENST00000463313.1:n.132+1del (TCTN1)
ENST00000464809.5:c.*896+1del (TCTN1)
ENST00000480648.5:c.*119+1del (TCTN1)
ENST00000482281.6:n.835+1del (TCTN1)
ENST00000490514.5:c.*667+1del (TCTN1)
ENST00000495659.6:c.*601+1del (TCTN1)
ENST00000548312.5:c.757-8325del (HVCN1) ENSP00000449601.1:n.757-8325del
ENST00000551555.2:n.513+1del (TCTN1)
ENST00000551590.5:c.843+1del (TCTN1)
ENST00000614115.4:c.801+1del (TCTN1)
NM_001082537.2:c.843+1del (TCTN1)
NM_001082538.2:c.843+1del (TCTN1)
NM_001173975.1:c.675+1del (TCTN1)
NM_001173976.1:c.663+1del (TCTN1)
NM_024549.5:c.801+1del (TCTN1)
XM_005253934.2:c.843+1del (TCTN1)
XM_005253935.2:c.843+1del (TCTN1)
XM_005253936.2:c.309+1del (TCTN1)
XM_006719594.1:c.675+1del (TCTN1)
XM_006719595.1:c.309+1del (TCTN1)
XM_006719596.1:c.309+1del (TCTN1)
XM_006719597.2:c.309+1del (TCTN1)
XM_006719598.1:c.309+1del (TCTN1)
XM_006719599.1:c.309+1del (TCTN1)
XM_006719600.1:c.309+1del (TCTN1)
XM_011538733.1:c.801+1del (TCTN1)
XM_011538734.1:c.783+1del (TCTN1)
XM_011538735.1:c.843+1del (TCTN1)
XM_011538736.1:c.843+1del (TCTN1)
XM_011538737.1:c.843+1del (TCTN1)
XM_011538738.1:c.843+1del (TCTN1)
XM_011538739.1:c.843+1del (TCTN1)
XR_243021.2:n.903+1del (TCTN1)
XR_243022.2:n.903+1del (TCTN1)
XR_429116.1:n.903+1del (TCTN1)
XR_944717.1:n.903+1del (TCTN1)
NM_001173975.2:c.675+1del (TCTN1)
NM_001319680.1:c.843+1del (TCTN1)
NM_001319681.1:c.309+1del (TCTN1)
NR_135088.1:n.1355+1del (TCTN1)
XM_005253934.4:c.843+1del (TCTN1)
XM_005253935.4:c.843+1del (TCTN1)
XM_006719594.3:c.675+1del (TCTN1)
XM_006719595.3:c.309+1del (TCTN1)
XM_006719596.3:c.309+1del (TCTN1)
XM_006719597.4:c.309+1del (TCTN1)
XM_006719598.3:c.309+1del (TCTN1)
XM_006719599.3:c.309+1del (TCTN1)
XM_006719600.3:c.309+1del (TCTN1)
XM_011538733.3:c.801+1del (TCTN1)
XM_011538734.3:c.783+1del (TCTN1)
XM_011538735.2:c.843+1del (TCTN1)
XM_011538737.3:c.843+1del (TCTN1)
XM_011538738.3:c.843+1del (TCTN1)
XM_017019964.1:c.675+1del (TCTN1)
XM_017019966.2:c.309+1del (TCTN1)
XM_017019968.2:c.309+1del (TCTN1)
XM_017019969.2:c.267+1del (TCTN1)
XR_243021.4:n.897+1del (TCTN1)
XR_243022.4:n.897+1del (TCTN1)
XR_429116.3:n.897+1del (TCTN1)
XR_944717.3:n.897+1del (TCTN1)
NM_001082537.3:c.843+1del (TCTN1)
NM_001082538.3:c.843+1del (TCTN1)
NM_001173975.3:c.675+1del (TCTN1)
NM_001173976.2:c.663+1del (TCTN1)
NM_001319680.2:c.843+1del (TCTN1)
NM_001319681.2:c.309+1del (TCTN1)
NM_024549.6:c.801+1del (TCTN1)
NR_135088.2:n.1253+1del (TCTN1)