Canonical Allele Identifier: CA10184679
Gene: TCN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.30614418_30614419del , CM000684.2:g.30614418_30614419del GRCh38
NC_000022.10:g.31010405_31010406del , CM000684.1:g.31010405_31010406del GRCh37
NC_000022.9:g.29340405_29340406del NCBI36
NG_007263.1:g.12245_12246del , LRG_116:g.12245_12246del

Transcript Alleles

HGVS Amino-acid Change
ENST00000471659.2:n.1974_1975del
ENST00000698263.1:c.497_498del ENSP00000513635.1:p.Leu166ProfsTer7
ENST00000698264.1:n.1974_1975del
ENST00000698265.1:c.497_498del ENSP00000513636.1:p.Leu166ProfsTer7
ENST00000698266.1:c.497_498del ENSP00000513637.1:p.Leu166ProfsTer7
ENST00000698267.1:c.497_498del ENSP00000513638.1:p.Leu166ProfsTer7
ENST00000698268.1:c.497_498del ENSP00000513639.1:p.Leu166ProfsTer7
ENST00000698269.1:c.*63_*64del ENSP00000513640.1:n.*63_*64del
ENST00000698270.1:c.428-883_428-882del ENSP00000513641.1:n.428-883_428-882del
ENST00000698271.1:c.497_498del ENSP00000513642.1:p.Leu166ProfsTer7
ENST00000698272.1:c.497_498del ENSP00000513643.1:p.Leu166ProfsTer7
ENST00000698273.1:c.488_489del ENSP00000513644.1:p.Leu163ProfsTer7
ENST00000215838.8:c.497_498del MANE Select ENSP00000215838.3:p.Leu166ProfsTer7
ENST00000215838.7:c.497_498del ENSP00000215838.3:p.Leu166ProfsTer7
ENST00000405742.7:c.485_486del ENSP00000385914.3:p.Leu162ProfsTer7
ENST00000407817.3:c.416_417del ENSP00000384914.3:p.Leu139ProfsTer7
ENST00000450638.5:c.422_423del ENSP00000394184.2:p.Leu141ProfsTer7
NM_000355.3:c.497_498del NP_000346.2:p.Leu166ProfsTer7
NM_001184726.1:c.416_417del NP_001171655.1:p.Leu139ProfsTer7
NM_000355.4:c.497_498del MANE Select NP_000346.2:p.Leu166ProfsTer7
NM_001184726.2:c.416_417del NP_001171655.1:p.Leu139ProfsTer7
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