Canonical Allele Identifier: CA639388193

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30614331dup , CM000684.2:g.30614331dup	GRCh38
NC_000022.10:g.31010318dup , CM000684.1:g.31010318dup	GRCh37
NC_000022.9:g.29340318dup	NCBI36
NG_007263.1:g.12158dup , LRG_116:g.12158dup

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.428-18dup MANE Select	NP_000346.2:n.428-18dup
ENST00000215838.8:c.428-18dup MANE Select	ENSP00000215838.3:n.428-18dup
NM_000355.3:c.428-18dup	NP_000346.2:n.428-18dup
NM_001184726.1:c.347-18dup	NP_001171655.1:n.347-18dup
NM_001184726.2:c.347-18dup	NP_001171655.1:n.347-18dup
ENST00000215838.7:c.428-18dup	ENSP00000215838.3:n.428-18dup
ENST00000405742.7:c.416-18dup	ENSP00000385914.3:n.416-18dup
ENST00000407817.3:c.347-18dup	ENSP00000384914.3:n.347-18dup
ENST00000450638.5:c.353-18dup	ENSP00000394184.2:n.353-18dup
ENST00000471659.2:n.1887dup
ENST00000698263.1:c.428-18dup	ENSP00000513635.1:n.428-18dup
ENST00000698264.1:n.1887dup
ENST00000698265.1:c.428-18dup	ENSP00000513636.1:n.428-18dup
ENST00000698266.1:c.428-18dup	ENSP00000513637.1:n.428-18dup
ENST00000698267.1:c.428-18dup	ENSP00000513638.1:n.428-18dup
ENST00000698268.1:c.428-18dup	ENSP00000513639.1:n.428-18dup
ENST00000698269.1:c.258-18dup	ENSP00000513640.1:n.258-18dup
ENST00000698270.1:c.428-970dup	ENSP00000513641.1:n.428-970dup
ENST00000698271.1:c.428-18dup	ENSP00000513642.1:n.428-18dup
ENST00000698272.1:c.428-18dup	ENSP00000513643.1:n.428-18dup
ENST00000698273.1:c.419-18dup	ENSP00000513644.1:n.419-18dup