Canonical Allele Identifier: CA10184850

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30615631G>C , CM000684.2:g.30615631G>C	GRCh38
NC_000022.10:g.31011618G>C , CM000684.1:g.31011618G>C	GRCh37
NC_000022.9:g.29341618G>C	NCBI36
NG_007263.1:g.13458G>C , LRG_116:g.13458G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.784G>C MANE Select	NP_000346.2:p.Glu262Gln
ENST00000215838.8:c.784G>C MANE Select	ENSP00000215838.3:p.Glu262Gln
NM_000355.3:c.784G>C	NP_000346.2:p.Glu262Gln
NM_001184726.1:c.703G>C	NP_001171655.1:p.Glu235Gln
NM_001184726.2:c.703G>C	NP_001171655.1:p.Glu235Gln
ENST00000215838.7:c.784G>C	ENSP00000215838.3:p.Glu262Gln
ENST00000405742.7:c.772G>C	ENSP00000385914.3:p.Glu258Gln
ENST00000407817.3:c.703G>C	ENSP00000384914.3:p.Glu235Gln
ENST00000450638.5:c.709G>C	ENSP00000394184.2:p.Glu237Gln
ENST00000471659.2:n.2261G>C
ENST00000698263.1:c.784G>C	ENSP00000513635.1:p.Glu262Gln
ENST00000698264.1:n.2261G>C
ENST00000698265.1:c.784G>C	ENSP00000513636.1:p.Glu262Gln
ENST00000698266.1:c.784G>C	ENSP00000513637.1:p.Glu262Gln
ENST00000698267.1:c.784G>C	ENSP00000513638.1:p.Glu262Gln
ENST00000698268.1:c.784G>C	ENSP00000513639.1:p.Glu262Gln
ENST00000698269.1:c.*350G>C	ENSP00000513640.1:n.*350G>C
ENST00000698270.1:c.631G>C	ENSP00000513641.1:p.Glu211Gln
ENST00000698271.1:c.814G>C	ENSP00000513642.1:p.Glu272Gln
ENST00000698272.1:c.775G>C	ENSP00000513643.1:p.Glu259Gln
ENST00000698273.1:c.775G>C	ENSP00000513644.1:p.Glu259Gln