Canonical Allele Identifier: CA10185017

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30623057G>A , CM000684.2:g.30623057G>A	GRCh38
NC_000022.10:g.31019044G>A , CM000684.1:g.31019044G>A	GRCh37
NC_000022.9:g.29349044G>A	NCBI36
NG_007263.1:g.20884G>A , LRG_116:g.20884G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471659.2:n.3287G>A
ENST00000698263.1:c.1107-3403G>A	ENSP00000513635.1:n.1107-3403G>A
ENST00000698264.1:n.2932G>A
ENST00000698265.1:c.1181G>A	ENSP00000513636.1:p.Arg394Gln
ENST00000698266.1:c.1196G>A	ENSP00000513637.1:p.Arg399Gln
ENST00000698267.1:c.*52G>A	ENSP00000513638.1:n.*52G>A
ENST00000698268.1:c.1223G>A	ENSP00000513639.1:p.Arg408Gln
ENST00000698269.1:c.*762G>A	ENSP00000513640.1:n.*762G>A
ENST00000698270.1:c.1043G>A	ENSP00000513641.1:p.Arg348Gln
ENST00000698271.1:c.1226G>A	ENSP00000513642.1:p.Arg409Gln
ENST00000698272.1:c.1187G>A	ENSP00000513643.1:p.Arg396Gln
ENST00000698273.1:c.1187G>A	ENSP00000513644.1:p.Arg396Gln
ENST00000215838.8:c.1196G>A MANE Select	ENSP00000215838.3:p.Arg399Gln
ENST00000215838.7:c.1196G>A	ENSP00000215838.3:p.Arg399Gln
ENST00000405742.7:c.1184G>A	ENSP00000385914.3:p.Arg395Gln
ENST00000407817.3:c.1115G>A	ENSP00000384914.3:p.Arg372Gln
ENST00000450638.5:c.1121G>A	ENSP00000394184.2:p.Arg374Gln
ENST00000493542.1:n.328G>A
NM_000355.3:c.1196G>A	NP_000346.2:p.Arg399Gln
NM_001184726.1:c.1115G>A	NP_001171655.1:p.Arg372Gln
NM_000355.4:c.1196G>A MANE Select	NP_000346.2:p.Arg399Gln
NM_001184726.2:c.1115G>A	NP_001171655.1:p.Arg372Gln