Canonical Allele Identifier: CA411215847

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30617488G>C , CM000684.2:g.30617488G>C	GRCh38
NC_000022.10:g.31013475G>C , CM000684.1:g.31013475G>C	GRCh37
NC_000022.9:g.29343475G>C	NCBI36
NG_007263.1:g.15315G>C , LRG_116:g.15315G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.1099G>C MANE Select	NP_000346.2:p.Gly367Arg
ENST00000215838.8:c.1099G>C MANE Select	ENSP00000215838.3:p.Gly367Arg
NM_000355.3:c.1099G>C	NP_000346.2:p.Gly367Arg
NM_001184726.1:c.1018G>C	NP_001171655.1:p.Gly340Arg
NM_001184726.2:c.1018G>C	NP_001171655.1:p.Gly340Arg
ENST00000215838.7:c.1099G>C	ENSP00000215838.3:p.Gly367Arg
ENST00000405742.7:c.1087G>C	ENSP00000385914.3:p.Gly363Arg
ENST00000407817.3:c.1018G>C	ENSP00000384914.3:p.Gly340Arg
ENST00000450638.5:c.1024G>C	ENSP00000394184.2:p.Gly342Arg
ENST00000471659.1:n.255G>C
ENST00000471659.2:n.2576G>C
ENST00000493542.1:n.231G>C
ENST00000698263.1:c.1099G>C	ENSP00000513635.1:p.Gly367Arg
ENST00000698264.1:n.2576G>C
ENST00000698265.1:c.1091+8G>C	ENSP00000513636.1:n.1091+8G>C
ENST00000698266.1:c.1099G>C	ENSP00000513637.1:p.Gly367Arg
ENST00000698267.1:c.940+1701G>C	ENSP00000513638.1:n.940+1701G>C
ENST00000698268.1:c.1126G>C	ENSP00000513639.1:p.Gly376Arg
ENST00000698269.1:c.*665G>C	ENSP00000513640.1:n.*665G>C
ENST00000698270.1:c.946G>C	ENSP00000513641.1:p.Gly316Arg
ENST00000698271.1:c.1129G>C	ENSP00000513642.1:p.Gly377Arg
ENST00000698272.1:c.1090G>C	ENSP00000513643.1:p.Gly364Arg
ENST00000698273.1:c.1090G>C	ENSP00000513644.1:p.Gly364Arg