Canonical Allele Identifier: CA1025006656

Gene: TCN2

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30622574T>A , CM000684.2:g.30622574T>A	GRCh38
NC_000022.10:g.31018561T>A , CM000684.1:g.31018561T>A	GRCh37
NC_000022.9:g.29348561T>A	NCBI36
NG_007263.1:g.20401T>A , LRG_116:g.20401T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471659.2:n.3198-394T>A
ENST00000698263.1:c.1107-3886T>A	ENSP00000513635.1:n.1107-3886T>A
ENST00000698264.1:n.2843-394T>A
ENST00000698265.1:c.1092-394T>A	ENSP00000513636.1:n.1092-394T>A
ENST00000698266.1:c.1107-394T>A	ENSP00000513637.1:n.1107-394T>A
ENST00000698267.1:c.941-394T>A	ENSP00000513638.1:n.941-394T>A
ENST00000698268.1:c.1134-394T>A	ENSP00000513639.1:n.1134-394T>A
ENST00000698269.1:c.*673-394T>A	ENSP00000513640.1:n.*673-394T>A
ENST00000698270.1:c.954-394T>A	ENSP00000513641.1:n.954-394T>A
ENST00000698271.1:c.1137-394T>A	ENSP00000513642.1:n.1137-394T>A
ENST00000698272.1:c.1098-394T>A	ENSP00000513643.1:n.1098-394T>A
ENST00000698273.1:c.1098-394T>A	ENSP00000513644.1:n.1098-394T>A
ENST00000215838.8:c.1107-394T>A MANE Select	ENSP00000215838.3:n.1107-394T>A
ENST00000215838.7:c.1107-394T>A	ENSP00000215838.3:n.1107-394T>A
ENST00000405742.7:c.1095-394T>A	ENSP00000385914.3:n.1095-394T>A
ENST00000407817.3:c.1026-394T>A	ENSP00000384914.3:n.1026-394T>A
ENST00000450638.5:c.1032-394T>A	ENSP00000394184.2:n.1032-394T>A
ENST00000493542.1:n.239-394T>A
NM_000355.3:c.1107-394T>A	NP_000346.2:n.1107-394T>A
NM_001184726.1:c.1026-394T>A	NP_001171655.1:n.1026-394T>A
NM_000355.4:c.1107-394T>A MANE Select	NP_000346.2:n.1107-394T>A
NM_001184726.2:c.1026-394T>A	NP_001171655.1:n.1026-394T>A