Canonical Allele Identifier: CA2401110033
Gene: TCN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.30612955G= , CM000684.2:g.30612955G= GRCh38
NC_000022.10:g.31008942G= , CM000684.1:g.31008942G= GRCh37
NC_000022.9:g.29338942G= NCBI36
NG_007263.1:g.10782G= , LRG_116:g.10782G=

Transcript Alleles

HGVS Amino-acid change
ENST00000471659.2:n.511G=
ENST00000698263.1:c.340G= ENSP00000513635.1:p.Ala114=
ENST00000698264.1:n.511G=
ENST00000698265.1:c.340G= ENSP00000513636.1:p.Ala114=
ENST00000698266.1:c.340G= ENSP00000513637.1:p.Ala114=
ENST00000698267.1:c.340G= ENSP00000513638.1:p.Ala114=
ENST00000698268.1:c.340G= ENSP00000513639.1:p.Ala114=
ENST00000698269.1:c.258-1394G= ENSP00000513640.1:n.258-1394G=
ENST00000698270.1:c.340G= ENSP00000513641.1:p.Ala114=
ENST00000698271.1:c.340G= ENSP00000513642.1:p.Ala114=
ENST00000698272.1:c.340G= ENSP00000513643.1:p.Ala114=
ENST00000698273.1:c.331G= ENSP00000513644.1:p.Ala111=
ENST00000215838.8:c.340G= MANE Select ENSP00000215838.3:p.Ala114=
ENST00000215838.7:c.340G= ENSP00000215838.3:p.Ala114=
ENST00000405742.7:c.328G= ENSP00000385914.3:p.Ala110=
ENST00000407817.3:c.340G= ENSP00000384914.3:p.Ala114=
ENST00000450638.5:c.265G= ENSP00000394184.2:p.Ala89=
NM_000355.3:c.340G= NP_000346.2:p.Ala114=
NM_001184726.1:c.340G= NP_001171655.1:p.Ala114=
NM_000355.4:c.340G= MANE Select NP_000346.2:p.Ala114=
NM_001184726.2:c.340G= NP_001171655.1:p.Ala114=