Canonical Allele Identifier: CA10185067

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30626474A>G , CM000684.2:g.30626474A>G	GRCh38
NC_000022.10:g.31022461A>G , CM000684.1:g.31022461A>G	GRCh37
NC_000022.9:g.29352461A>G	NCBI36
NG_007263.1:g.24301A>G , LRG_116:g.24301A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.1237A>G MANE Select	NP_000346.2:p.Arg413Gly
ENST00000215838.8:c.1237A>G MANE Select	ENSP00000215838.3:p.Arg413Gly
NM_000355.3:c.1237A>G	NP_000346.2:p.Arg413Gly
NM_001184726.1:c.1156A>G	NP_001171655.1:p.Arg386Gly
NM_001184726.2:c.1156A>G	NP_001171655.1:p.Arg386Gly
ENST00000215838.7:c.1237A>G	ENSP00000215838.3:p.Arg413Gly
ENST00000405742.7:c.1225A>G	ENSP00000385914.3:p.Arg409Gly
ENST00000407817.3:c.1156A>G	ENSP00000384914.3:p.Arg386Gly
ENST00000450638.5:c.1162A>G	ENSP00000394184.2:p.Arg388Gly
ENST00000471659.2:n.3328A>G
ENST00000698263.1:c.*5A>G	ENSP00000513635.1:n.*5A>G
ENST00000698264.1:n.2973A>G
ENST00000698265.1:c.1222A>G	ENSP00000513636.1:p.Arg408Gly
ENST00000698266.1:c.*63A>G	ENSP00000513637.1:n.*63A>G
ENST00000698267.1:c.*93A>G	ENSP00000513638.1:n.*93A>G
ENST00000698268.1:c.1264A>G	ENSP00000513639.1:p.Arg422Gly
ENST00000698269.1:c.*803A>G	ENSP00000513640.1:n.*803A>G
ENST00000698270.1:c.1084A>G	ENSP00000513641.1:p.Arg362Gly
ENST00000698271.1:c.1267A>G	ENSP00000513642.1:p.Arg423Gly
ENST00000698272.1:c.1228A>G	ENSP00000513643.1:p.Arg410Gly
ENST00000698273.1:c.1228A>G	ENSP00000513644.1:p.Arg410Gly