Canonical Allele Identifier: CA1976606319
Gene: TCN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.59865967T= , CM000673.2:g.59865967T= GRCh38
NC_000011.9:g.59633440T= , CM000673.1:g.59633440T= GRCh37
NC_000011.8:g.59390016T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000257264.4:c.79+425A= MANE Select ENSP00000257264.3:n.79+425A=
ENST00000257264.3:c.79+425A= ENSP00000257264.3:n.79+425A=
ENST00000532419.5:n.98+425A=
ENST00000534531.1:n.80+425A=
NM_001062.3:c.79+425A= NP_001053.2:n.79+425A=
NM_001062.4:c.79+425A= MANE Select NP_001053.2:n.79+425A=
Search 100 bp 5'
Search 100 bp 3'