Canonical Allele Identifier: CA2401111673

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30615623G= , CM000684.2:g.30615623G=	GRCh38
NC_000022.10:g.31011610G= , CM000684.1:g.31011610G=	GRCh37
NC_000022.9:g.29341610G=	NCBI36
NG_007263.1:g.13450G= , LRG_116:g.13450G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.776G= MANE Select	NP_000346.2:p.Arg259=
ENST00000215838.8:c.776G= MANE Select	ENSP00000215838.3:p.Arg259=
NM_000355.3:c.776G=	NP_000346.2:p.Arg259=
NM_001184726.1:c.695G=	NP_001171655.1:p.Arg232=
NM_001184726.2:c.695G=	NP_001171655.1:p.Arg232=
ENST00000215838.7:c.776G=	ENSP00000215838.3:p.Arg259=
ENST00000405742.7:c.764G=	ENSP00000385914.3:p.Arg255=
ENST00000407817.3:c.695G=	ENSP00000384914.3:p.Arg232=
ENST00000450638.5:c.701G=	ENSP00000394184.2:p.Arg234=
ENST00000471659.2:n.2253G=
ENST00000698263.1:c.776G=	ENSP00000513635.1:p.Arg259=
ENST00000698264.1:n.2253G=
ENST00000698265.1:c.776G=	ENSP00000513636.1:p.Arg259=
ENST00000698266.1:c.776G=	ENSP00000513637.1:p.Arg259=
ENST00000698267.1:c.776G=	ENSP00000513638.1:p.Arg259=
ENST00000698268.1:c.776G=	ENSP00000513639.1:p.Arg259=
ENST00000698269.1:c.*342G=	ENSP00000513640.1:n.*342G=
ENST00000698270.1:c.623G=	ENSP00000513641.1:p.Arg208=
ENST00000698271.1:c.806G=	ENSP00000513642.1:p.Arg269=
ENST00000698272.1:c.767G=	ENSP00000513643.1:p.Arg256=
ENST00000698273.1:c.767G=	ENSP00000513644.1:p.Arg256=