Canonical Allele Identifier: CA10184666

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30614345T>C , CM000684.2:g.30614345T>C	GRCh38
NC_000022.10:g.31010332T>C , CM000684.1:g.31010332T>C	GRCh37
NC_000022.9:g.29340332T>C	NCBI36
NG_007263.1:g.12172T>C , LRG_116:g.12172T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.428-4T>C MANE Select	NP_000346.2:n.428-4T>C
ENST00000215838.8:c.428-4T>C MANE Select	ENSP00000215838.3:n.428-4T>C
NM_000355.3:c.428-4T>C	NP_000346.2:n.428-4T>C
NM_001184726.1:c.347-4T>C	NP_001171655.1:n.347-4T>C
NM_001184726.2:c.347-4T>C	NP_001171655.1:n.347-4T>C
ENST00000215838.7:c.428-4T>C	ENSP00000215838.3:n.428-4T>C
ENST00000405742.7:c.416-4T>C	ENSP00000385914.3:n.416-4T>C
ENST00000407817.3:c.347-4T>C	ENSP00000384914.3:n.347-4T>C
ENST00000450638.5:c.353-4T>C	ENSP00000394184.2:n.353-4T>C
ENST00000471659.2:n.1901T>C
ENST00000698263.1:c.428-4T>C	ENSP00000513635.1:n.428-4T>C
ENST00000698264.1:n.1901T>C
ENST00000698265.1:c.428-4T>C	ENSP00000513636.1:n.428-4T>C
ENST00000698266.1:c.428-4T>C	ENSP00000513637.1:n.428-4T>C
ENST00000698267.1:c.428-4T>C	ENSP00000513638.1:n.428-4T>C
ENST00000698268.1:c.428-4T>C	ENSP00000513639.1:n.428-4T>C
ENST00000698269.1:c.258-4T>C	ENSP00000513640.1:n.258-4T>C
ENST00000698270.1:c.428-956T>C	ENSP00000513641.1:n.428-956T>C
ENST00000698271.1:c.428-4T>C	ENSP00000513642.1:n.428-4T>C
ENST00000698272.1:c.428-4T>C	ENSP00000513643.1:n.428-4T>C
ENST00000698273.1:c.419-4T>C	ENSP00000513644.1:n.419-4T>C