Canonical Allele Identifier: CA10653353

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30617481G>A , CM000684.2:g.30617481G>A	GRCh38
NC_000022.10:g.31013468G>A , CM000684.1:g.31013468G>A	GRCh37
NC_000022.9:g.29343468G>A	NCBI36
NG_007263.1:g.15308G>A , LRG_116:g.15308G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.1092G>A MANE Select	NP_000346.2:p.Glu364=
ENST00000215838.8:c.1092G>A MANE Select	ENSP00000215838.3:p.Glu364=
NM_000355.3:c.1092G>A	NP_000346.2:p.Glu364=
NM_001184726.1:c.1011G>A	NP_001171655.1:p.Glu337=
NM_001184726.2:c.1011G>A	NP_001171655.1:p.Glu337=
ENST00000215838.7:c.1092G>A	ENSP00000215838.3:p.Glu364=
ENST00000405742.7:c.1080G>A	ENSP00000385914.3:p.Glu360=
ENST00000407817.3:c.1011G>A	ENSP00000384914.3:p.Glu337=
ENST00000450638.5:c.1017G>A	ENSP00000394184.2:p.Glu339=
ENST00000471659.1:n.248G>A
ENST00000471659.2:n.2569G>A
ENST00000493542.1:n.224G>A
ENST00000698263.1:c.1092G>A	ENSP00000513635.1:p.Glu364=
ENST00000698264.1:n.2569G>A
ENST00000698265.1:c.1091+1G>A	ENSP00000513636.1:n.1091+1G>A
ENST00000698266.1:c.1092G>A	ENSP00000513637.1:p.Glu364=
ENST00000698267.1:c.940+1694G>A	ENSP00000513638.1:n.940+1694G>A
ENST00000698268.1:c.1119G>A	ENSP00000513639.1:p.Glu373=
ENST00000698269.1:c.*658G>A	ENSP00000513640.1:n.*658G>A
ENST00000698270.1:c.939G>A	ENSP00000513641.1:p.Glu313=
ENST00000698271.1:c.1122G>A	ENSP00000513642.1:p.Glu374=
ENST00000698272.1:c.1083G>A	ENSP00000513643.1:p.Glu361=
ENST00000698273.1:c.1083G>A	ENSP00000513644.1:p.Glu361=