Canonical Allele Identifier: CA2573157910

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30615729del , CM000684.2:g.30615729del	GRCh38
NC_000022.10:g.31011716del , CM000684.1:g.31011716del	GRCh37
NC_000022.9:g.29341716del	NCBI36
NG_007263.1:g.13556del , LRG_116:g.13556del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471659.2:n.2359del
ENST00000698263.1:c.882del	ENSP00000513635.1:p.Val295PhefsTer2
ENST00000698264.1:n.2359del
ENST00000698265.1:c.882del	ENSP00000513636.1:p.Val295PhefsTer2
ENST00000698266.1:c.882del	ENSP00000513637.1:p.Val295PhefsTer2
ENST00000698267.1:c.882del	ENSP00000513638.1:p.Val295PhefsTer2
ENST00000698268.1:c.882del	ENSP00000513639.1:p.Val295PhefsTer2
ENST00000698269.1:c.*448del	ENSP00000513640.1:n.*448del
ENST00000698270.1:c.729del	ENSP00000513641.1:p.Val244PhefsTer2
ENST00000698271.1:c.912del	ENSP00000513642.1:p.Val305PhefsTer2
ENST00000698272.1:c.873del	ENSP00000513643.1:p.Val292PhefsTer2
ENST00000698273.1:c.873del	ENSP00000513644.1:p.Val292PhefsTer2
ENST00000215838.8:c.882del MANE Select	ENSP00000215838.3:p.Val295PhefsTer2
ENST00000215838.7:c.882del	ENSP00000215838.3:p.Val295PhefsTer2
ENST00000405742.7:c.870del	ENSP00000385914.3:p.Val291PhefsTer2
ENST00000407817.3:c.801del	ENSP00000384914.3:p.Val268PhefsTer2
ENST00000450638.5:c.807del	ENSP00000394184.2:p.Val270PhefsTer2
ENST00000471659.1:n.38del
ENST00000493542.1:n.14del
NM_000355.3:c.882del	NP_000346.2:p.Val295PhefsTer2
NM_001184726.1:c.801del	NP_001171655.1:p.Val268PhefsTer2
NM_000355.4:c.882del MANE Select	NP_000346.2:p.Val295PhefsTer2
NM_001184726.2:c.801del	NP_001171655.1:p.Val268PhefsTer2