Canonical Allele Identifier: CA2401110930

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30614430G= , CM000684.2:g.30614430G=	GRCh38
NC_000022.10:g.31010417G= , CM000684.1:g.31010417G=	GRCh37
NC_000022.9:g.29340417G=	NCBI36
NG_007263.1:g.12257G= , LRG_116:g.12257G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.509G= MANE Select	NP_000346.2:p.Arg170=
ENST00000215838.8:c.509G= MANE Select	ENSP00000215838.3:p.Arg170=
NM_000355.3:c.509G=	NP_000346.2:p.Arg170=
NM_001184726.1:c.428G=	NP_001171655.1:p.Arg143=
NM_001184726.2:c.428G=	NP_001171655.1:p.Arg143=
ENST00000215838.7:c.509G=	ENSP00000215838.3:p.Arg170=
ENST00000405742.7:c.497G=	ENSP00000385914.3:p.Arg166=
ENST00000407817.3:c.428G=	ENSP00000384914.3:p.Arg143=
ENST00000450638.5:c.434G=	ENSP00000394184.2:p.Arg145=
ENST00000471659.2:n.1986G=
ENST00000698263.1:c.509G=	ENSP00000513635.1:p.Arg170=
ENST00000698264.1:n.1986G=
ENST00000698265.1:c.509G=	ENSP00000513636.1:p.Arg170=
ENST00000698266.1:c.509G=	ENSP00000513637.1:p.Arg170=
ENST00000698267.1:c.509G=	ENSP00000513638.1:p.Arg170=
ENST00000698268.1:c.509G=	ENSP00000513639.1:p.Arg170=
ENST00000698269.1:c.*75G=	ENSP00000513640.1:n.*75G=
ENST00000698270.1:c.428-871G=	ENSP00000513641.1:n.428-871G=
ENST00000698271.1:c.509G=	ENSP00000513642.1:p.Arg170=
ENST00000698272.1:c.509G=	ENSP00000513643.1:p.Arg170=
ENST00000698273.1:c.500G=	ENSP00000513644.1:p.Arg167=