Canonical Allele Identifier: CA10184957

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30617478T>G , CM000684.2:g.30617478T>G	GRCh38
NC_000022.10:g.31013465T>G , CM000684.1:g.31013465T>G	GRCh37
NC_000022.9:g.29343465T>G	NCBI36
NG_007263.1:g.15305T>G , LRG_116:g.15305T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.1089T>G MANE Select	NP_000346.2:p.His363Gln
ENST00000215838.8:c.1089T>G MANE Select	ENSP00000215838.3:p.His363Gln
NM_000355.3:c.1089T>G	NP_000346.2:p.His363Gln
NM_001184726.1:c.1008T>G	NP_001171655.1:p.His336Gln
NM_001184726.2:c.1008T>G	NP_001171655.1:p.His336Gln
ENST00000215838.7:c.1089T>G	ENSP00000215838.3:p.His363Gln
ENST00000405742.7:c.1077T>G	ENSP00000385914.3:p.His359Gln
ENST00000407817.3:c.1008T>G	ENSP00000384914.3:p.His336Gln
ENST00000450638.5:c.1014T>G	ENSP00000394184.2:p.His338Gln
ENST00000471659.1:n.245T>G
ENST00000471659.2:n.2566T>G
ENST00000493542.1:n.221T>G
ENST00000698263.1:c.1089T>G	ENSP00000513635.1:p.His363Gln
ENST00000698264.1:n.2566T>G
ENST00000698265.1:c.1089T>G	ENSP00000513636.1:p.His363Gln
ENST00000698266.1:c.1089T>G	ENSP00000513637.1:p.His363Gln
ENST00000698267.1:c.940+1691T>G	ENSP00000513638.1:n.940+1691T>G
ENST00000698268.1:c.1116T>G	ENSP00000513639.1:p.His372Gln
ENST00000698269.1:c.*655T>G	ENSP00000513640.1:n.*655T>G
ENST00000698270.1:c.936T>G	ENSP00000513641.1:p.His312Gln
ENST00000698271.1:c.1119T>G	ENSP00000513642.1:p.His373Gln
ENST00000698272.1:c.1080T>G	ENSP00000513643.1:p.His360Gln
ENST00000698273.1:c.1080T>G	ENSP00000513644.1:p.His360Gln