Canonical Allele Identifier: CA411208657

Gene: TCN2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000471659.2:n.512C>T
ENST00000698263.1:c.341C>T	ENSP00000513635.1:p.Ala114Val
ENST00000698264.1:n.512C>T
ENST00000698265.1:c.341C>T	ENSP00000513636.1:p.Ala114Val
ENST00000698266.1:c.341C>T	ENSP00000513637.1:p.Ala114Val
ENST00000698267.1:c.341C>T	ENSP00000513638.1:p.Ala114Val
ENST00000698268.1:c.341C>T	ENSP00000513639.1:p.Ala114Val
ENST00000698269.1:c.258-1393C>T	ENSP00000513640.1:n.258-1393C>T
ENST00000698270.1:c.341C>T	ENSP00000513641.1:p.Ala114Val
ENST00000698271.1:c.341C>T	ENSP00000513642.1:p.Ala114Val
ENST00000698272.1:c.341C>T	ENSP00000513643.1:p.Ala114Val
ENST00000698273.1:c.332C>T	ENSP00000513644.1:p.Ala111Val
ENST00000215838.8:c.341C>T MANE Select	ENSP00000215838.3:p.Ala114Val
ENST00000215838.7:c.341C>T	ENSP00000215838.3:p.Ala114Val
ENST00000405742.7:c.329C>T	ENSP00000385914.3:p.Ala110Val
ENST00000407817.3:c.341C>T	ENSP00000384914.3:p.Ala114Val
ENST00000450638.5:c.266C>T	ENSP00000394184.2:p.Ala89Val
NM_000355.3:c.341C>T	NP_000346.2:p.Ala114Val
NM_001184726.1:c.341C>T	NP_001171655.1:p.Ala114Val
NM_000355.4:c.341C>T MANE Select	NP_000346.2:p.Ala114Val
NM_001184726.2:c.341C>T	NP_001171655.1:p.Ala114Val