Canonical Allele Identifier: CA411212956

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30615603C>A , CM000684.2:g.30615603C>A	GRCh38
NC_000022.10:g.31011590C>A , CM000684.1:g.31011590C>A	GRCh37
NC_000022.9:g.29341590C>A	NCBI36
NG_007263.1:g.13430C>A , LRG_116:g.13430C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.756C>A MANE Select	NP_000346.2:p.Phe252Leu
ENST00000215838.8:c.756C>A MANE Select	ENSP00000215838.3:p.Phe252Leu
NM_000355.3:c.756C>A	NP_000346.2:p.Phe252Leu
NM_001184726.1:c.675C>A	NP_001171655.1:p.Phe225Leu
NM_001184726.2:c.675C>A	NP_001171655.1:p.Phe225Leu
ENST00000215838.7:c.756C>A	ENSP00000215838.3:p.Phe252Leu
ENST00000405742.7:c.744C>A	ENSP00000385914.3:p.Phe248Leu
ENST00000407817.3:c.675C>A	ENSP00000384914.3:p.Phe225Leu
ENST00000450638.5:c.681C>A	ENSP00000394184.2:p.Phe227Leu
ENST00000471659.2:n.2233C>A
ENST00000698263.1:c.756C>A	ENSP00000513635.1:p.Phe252Leu
ENST00000698264.1:n.2233C>A
ENST00000698265.1:c.756C>A	ENSP00000513636.1:p.Phe252Leu
ENST00000698266.1:c.756C>A	ENSP00000513637.1:p.Phe252Leu
ENST00000698267.1:c.756C>A	ENSP00000513638.1:p.Phe252Leu
ENST00000698268.1:c.756C>A	ENSP00000513639.1:p.Phe252Leu
ENST00000698269.1:c.*322C>A	ENSP00000513640.1:n.*322C>A
ENST00000698270.1:c.603C>A	ENSP00000513641.1:p.Phe201Leu
ENST00000698271.1:c.786C>A	ENSP00000513642.1:p.Phe262Leu
ENST00000698272.1:c.747C>A	ENSP00000513643.1:p.Phe249Leu
ENST00000698273.1:c.747C>A	ENSP00000513644.1:p.Phe249Leu