Canonical Allele Identifier: CA2695230567

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30612945dup , CM000684.2:g.30612945dup	GRCh38
NC_000022.10:g.31008932dup , CM000684.1:g.31008932dup	GRCh37
NC_000022.9:g.29338932dup	NCBI36
NG_007263.1:g.10772dup , LRG_116:g.10772dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471659.2:n.501dup
ENST00000698263.1:c.330dup	ENSP00000513635.1:p.Ala111ArgfsTer7
ENST00000698264.1:n.501dup
ENST00000698265.1:c.330dup	ENSP00000513636.1:p.Ala111ArgfsTer7
ENST00000698266.1:c.330dup	ENSP00000513637.1:p.Ala111ArgfsTer7
ENST00000698267.1:c.330dup	ENSP00000513638.1:p.Ala111ArgfsTer7
ENST00000698268.1:c.330dup	ENSP00000513639.1:p.Ala111ArgfsTer7
ENST00000698269.1:c.258-1404dup	ENSP00000513640.1:n.258-1404dup
ENST00000698270.1:c.330dup	ENSP00000513641.1:p.Ala111ArgfsTer7
ENST00000698271.1:c.330dup	ENSP00000513642.1:p.Ala111ArgfsTer7
ENST00000698272.1:c.330dup	ENSP00000513643.1:p.Ala111ArgfsTer7
ENST00000698273.1:c.321dup	ENSP00000513644.1:p.Ala108ArgfsTer7
ENST00000215838.8:c.330dup MANE Select	ENSP00000215838.3:p.Ala111ArgfsTer7
ENST00000215838.7:c.330dup	ENSP00000215838.3:p.Ala111ArgfsTer7
ENST00000405742.7:c.318dup	ENSP00000385914.3:p.Ala107ArgfsTer7
ENST00000407817.3:c.330dup	ENSP00000384914.3:p.Ala111ArgfsTer8
ENST00000450638.5:c.255dup	ENSP00000394184.2:p.Ala86ArgfsTer7
NM_000355.3:c.330dup	NP_000346.2:p.Ala111ArgfsTer7
NM_001184726.1:c.330dup	NP_001171655.1:p.Ala111ArgfsTer8
NM_000355.4:c.330dup MANE Select	NP_000346.2:p.Ala111ArgfsTer7
NM_001184726.2:c.330dup	NP_001171655.1:p.Ala111ArgfsTer8