Canonical Allele Identifier: CA411207849

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30612872G>A , CM000684.2:g.30612872G>A	GRCh38
NC_000022.10:g.31008859G>A , CM000684.1:g.31008859G>A	GRCh37
NC_000022.9:g.29338859G>A	NCBI36
NG_007263.1:g.10699G>A , LRG_116:g.10699G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.258-1G>A MANE Select	NP_000346.2:n.258-1G>A
ENST00000215838.8:c.258-1G>A MANE Select	ENSP00000215838.3:n.258-1G>A
NM_000355.3:c.258-1G>A	NP_000346.2:n.258-1G>A
NM_001184726.1:c.258-1G>A	NP_001171655.1:n.258-1G>A
NM_001184726.2:c.258-1G>A	NP_001171655.1:n.258-1G>A
ENST00000215838.7:c.258-1G>A	ENSP00000215838.3:n.258-1G>A
ENST00000405742.7:c.258-13G>A	ENSP00000385914.3:n.258-13G>A
ENST00000407817.3:c.258-1G>A	ENSP00000384914.3:n.258-1G>A
ENST00000450638.5:c.183-1G>A	ENSP00000394184.2:n.183-1G>A
ENST00000471659.2:n.429-1G>A
ENST00000698263.1:c.258-1G>A	ENSP00000513635.1:n.258-1G>A
ENST00000698264.1:n.429-1G>A
ENST00000698265.1:c.258-1G>A	ENSP00000513636.1:n.258-1G>A
ENST00000698266.1:c.258-1G>A	ENSP00000513637.1:n.258-1G>A
ENST00000698267.1:c.258-1G>A	ENSP00000513638.1:n.258-1G>A
ENST00000698268.1:c.258-1G>A	ENSP00000513639.1:n.258-1G>A
ENST00000698269.1:c.258-1477G>A	ENSP00000513640.1:n.258-1477G>A
ENST00000698270.1:c.258-1G>A	ENSP00000513641.1:n.258-1G>A
ENST00000698271.1:c.258-1G>A	ENSP00000513642.1:n.258-1G>A
ENST00000698272.1:c.258-1G>A	ENSP00000513643.1:n.258-1G>A
ENST00000698273.1:c.249-1G>A	ENSP00000513644.1:n.249-1G>A