Canonical Allele Identifier: CA411215018

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30617328A>G , CM000684.2:g.30617328A>G	GRCh38
NC_000022.10:g.31013315A>G , CM000684.1:g.31013315A>G	GRCh37
NC_000022.9:g.29343315A>G	NCBI36
NG_007263.1:g.15155A>G , LRG_116:g.15155A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.941-2A>G MANE Select	NP_000346.2:n.941-2A>G
ENST00000215838.8:c.941-2A>G MANE Select	ENSP00000215838.3:n.941-2A>G
NM_000355.3:c.941-2A>G	NP_000346.2:n.941-2A>G
NM_001184726.1:c.860-2A>G	NP_001171655.1:n.860-2A>G
NM_001184726.2:c.860-2A>G	NP_001171655.1:n.860-2A>G
ENST00000215838.7:c.941-2A>G	ENSP00000215838.3:n.941-2A>G
ENST00000405742.7:c.929-2A>G	ENSP00000385914.3:n.929-2A>G
ENST00000407817.3:c.860-2A>G	ENSP00000384914.3:n.860-2A>G
ENST00000450638.5:c.866-2A>G	ENSP00000394184.2:n.866-2A>G
ENST00000471659.1:n.97-2A>G
ENST00000471659.2:n.2418-2A>G
ENST00000493542.1:n.73-2A>G
ENST00000698263.1:c.941-2A>G	ENSP00000513635.1:n.941-2A>G
ENST00000698264.1:n.2418-2A>G
ENST00000698265.1:c.941-2A>G	ENSP00000513636.1:n.941-2A>G
ENST00000698266.1:c.941-2A>G	ENSP00000513637.1:n.941-2A>G
ENST00000698267.1:c.940+1541A>G	ENSP00000513638.1:n.940+1541A>G
ENST00000698268.1:c.966A>G	ENSP00000513639.1:p.Thr322=
ENST00000698269.1:c.*507-2A>G	ENSP00000513640.1:n.*507-2A>G
ENST00000698270.1:c.788-2A>G	ENSP00000513641.1:n.788-2A>G
ENST00000698271.1:c.971-2A>G	ENSP00000513642.1:n.971-2A>G
ENST00000698272.1:c.932-2A>G	ENSP00000513643.1:n.932-2A>G
ENST00000698273.1:c.932-2A>G	ENSP00000513644.1:n.932-2A>G