Canonical Allele Identifier: CA10184913
Gene: TCN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.30617309G>A , CM000684.2:g.30617309G>A GRCh38
NC_000022.10:g.31013296G>A , CM000684.1:g.31013296G>A GRCh37
NC_000022.9:g.29343296G>A NCBI36
NG_007263.1:g.15136G>A , LRG_116:g.15136G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000471659.2:n.2418-21G>A
ENST00000698263.1:c.941-21G>A ENSP00000513635.1:n.941-21G>A
ENST00000698264.1:n.2418-21G>A
ENST00000698265.1:c.941-21G>A ENSP00000513636.1:n.941-21G>A
ENST00000698266.1:c.941-21G>A ENSP00000513637.1:n.941-21G>A
ENST00000698267.1:c.940+1522G>A ENSP00000513638.1:n.940+1522G>A
ENST00000698268.1:c.947G>A ENSP00000513639.1:p.Arg316His
ENST00000698269.1:c.*507-21G>A ENSP00000513640.1:n.*507-21G>A
ENST00000698270.1:c.788-21G>A ENSP00000513641.1:n.788-21G>A
ENST00000698271.1:c.971-21G>A ENSP00000513642.1:n.971-21G>A
ENST00000698272.1:c.932-21G>A ENSP00000513643.1:n.932-21G>A
ENST00000698273.1:c.932-21G>A ENSP00000513644.1:n.932-21G>A
ENST00000215838.8:c.941-21G>A MANE Select ENSP00000215838.3:n.941-21G>A
ENST00000215838.7:c.941-21G>A ENSP00000215838.3:n.941-21G>A
ENST00000405742.7:c.929-21G>A ENSP00000385914.3:n.929-21G>A
ENST00000407817.3:c.860-21G>A ENSP00000384914.3:n.860-21G>A
ENST00000450638.5:c.866-21G>A ENSP00000394184.2:n.866-21G>A
ENST00000471659.1:n.97-21G>A
ENST00000493542.1:n.73-21G>A
NM_000355.3:c.941-21G>A NP_000346.2:n.941-21G>A
NM_001184726.1:c.860-21G>A NP_001171655.1:n.860-21G>A
NM_000355.4:c.941-21G>A MANE Select NP_000346.2:n.941-21G>A
NM_001184726.2:c.860-21G>A NP_001171655.1:n.860-21G>A
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