Canonical Allele Identifier: CA411208649

Gene: TCN2

Linked Data

• MyVariant Identifiers: chr22:g.31008943C>A (hg19) ; chr22:g.30612956C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30612956C>A , CM000684.2:g.30612956C>A	GRCh38
NC_000022.10:g.31008943C>A , CM000684.1:g.31008943C>A	GRCh37
NC_000022.9:g.29338943C>A	NCBI36
NG_007263.1:g.10783C>A , LRG_116:g.10783C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471659.2:n.512C>A
ENST00000698263.1:c.341C>A	ENSP00000513635.1:p.Ala114Asp
ENST00000698264.1:n.512C>A
ENST00000698265.1:c.341C>A	ENSP00000513636.1:p.Ala114Asp
ENST00000698266.1:c.341C>A	ENSP00000513637.1:p.Ala114Asp
ENST00000698267.1:c.341C>A	ENSP00000513638.1:p.Ala114Asp
ENST00000698268.1:c.341C>A	ENSP00000513639.1:p.Ala114Asp
ENST00000698269.1:c.258-1393C>A	ENSP00000513640.1:n.258-1393C>A
ENST00000698270.1:c.341C>A	ENSP00000513641.1:p.Ala114Asp
ENST00000698271.1:c.341C>A	ENSP00000513642.1:p.Ala114Asp
ENST00000698272.1:c.341C>A	ENSP00000513643.1:p.Ala114Asp
ENST00000698273.1:c.332C>A	ENSP00000513644.1:p.Ala111Asp
ENST00000215838.8:c.341C>A MANE Select	ENSP00000215838.3:p.Ala114Asp
ENST00000215838.7:c.341C>A	ENSP00000215838.3:p.Ala114Asp
ENST00000405742.7:c.329C>A	ENSP00000385914.3:p.Ala110Asp
ENST00000407817.3:c.341C>A	ENSP00000384914.3:p.Ala114Asp
ENST00000450638.5:c.266C>A	ENSP00000394184.2:p.Ala89Asp
NM_000355.3:c.341C>A	NP_000346.2:p.Ala114Asp
NM_001184726.1:c.341C>A	NP_001171655.1:p.Ala114Asp
NM_000355.4:c.341C>A MANE Select	NP_000346.2:p.Ala114Asp
NM_001184726.2:c.341C>A	NP_001171655.1:p.Ala114Asp