Canonical Allele Identifier: CA204381

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30615774_30615777del , CM000684.2:g.30615774_30615777del	GRCh38
NC_000022.10:g.31011761_31011764del , CM000684.1:g.31011761_31011764del	GRCh37
NC_000022.9:g.29341761_29341764del	NCBI36
NG_007263.1:g.13601_13604del , LRG_116:g.13601_13604del

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.927_930del MANE Select	NP_000346.2:p.Cys309TrpfsTer?
ENST00000215838.8:c.927_930del MANE Select	ENSP00000215838.3:p.Cys309TrpfsTer?
NM_000355.3:c.927_930del	NP_000346.2:p.Cys309TrpfsTer?
NM_001184726.1:c.846_849del	NP_001171655.1:p.Cys282TrpfsTer?
NM_001184726.2:c.846_849del	NP_001171655.1:p.Cys282TrpfsTer?
ENST00000215838.7:c.927_930del	ENSP00000215838.3:p.Cys309TrpfsTer?
ENST00000405742.7:c.915_918del	ENSP00000385914.3:p.Cys305TrpfsTer?
ENST00000407817.3:c.846_849del	ENSP00000384914.3:p.Cys282TrpfsTer?
ENST00000450638.5:c.852_855del	ENSP00000394184.2:p.Cys284TrpfsTer?
ENST00000471659.1:n.83_86del
ENST00000471659.2:n.2404_2407del
ENST00000493542.1:n.59_62del
ENST00000698263.1:c.927_930del	ENSP00000513635.1:p.Cys309TrpfsTer?
ENST00000698264.1:n.2404_2407del
ENST00000698265.1:c.927_930del	ENSP00000513636.1:p.Cys309TrpfsTer?
ENST00000698266.1:c.927_930del	ENSP00000513637.1:p.Cys309TrpfsTer?
ENST00000698267.1:c.927_930del	ENSP00000513638.1:p.Cys309TrpfsTer6
ENST00000698268.1:c.927_930del	ENSP00000513639.1:p.Cys309TrpfsTer?
ENST00000698269.1:c.*493_*496del	ENSP00000513640.1:n.*493_*496del
ENST00000698270.1:c.774_777del	ENSP00000513641.1:p.Cys258TrpfsTer?
ENST00000698271.1:c.957_960del	ENSP00000513642.1:p.Cys319TrpfsTer?
ENST00000698272.1:c.918_921del	ENSP00000513643.1:p.Cys306TrpfsTer?
ENST00000698273.1:c.918_921del	ENSP00000513644.1:p.Cys306TrpfsTer?