Canonical Allele Identifier: CA10184669

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30614369C>G , CM000684.2:g.30614369C>G	GRCh38
NC_000022.10:g.31010356C>G , CM000684.1:g.31010356C>G	GRCh37
NC_000022.9:g.29340356C>G	NCBI36
NG_007263.1:g.12196C>G , LRG_116:g.12196C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.448C>G MANE Select	NP_000346.2:p.Pro150Ala
ENST00000215838.8:c.448C>G MANE Select	ENSP00000215838.3:p.Pro150Ala
NM_000355.3:c.448C>G	NP_000346.2:p.Pro150Ala
NM_001184726.1:c.367C>G	NP_001171655.1:p.Pro123Ala
NM_001184726.2:c.367C>G	NP_001171655.1:p.Pro123Ala
ENST00000215838.7:c.448C>G	ENSP00000215838.3:p.Pro150Ala
ENST00000405742.7:c.436C>G	ENSP00000385914.3:p.Pro146Ala
ENST00000407817.3:c.367C>G	ENSP00000384914.3:p.Pro123Ala
ENST00000450638.5:c.373C>G	ENSP00000394184.2:p.Pro125Ala
ENST00000471659.2:n.1925C>G
ENST00000698263.1:c.448C>G	ENSP00000513635.1:p.Pro150Ala
ENST00000698264.1:n.1925C>G
ENST00000698265.1:c.448C>G	ENSP00000513636.1:p.Pro150Ala
ENST00000698266.1:c.448C>G	ENSP00000513637.1:p.Pro150Ala
ENST00000698267.1:c.448C>G	ENSP00000513638.1:p.Pro150Ala
ENST00000698268.1:c.448C>G	ENSP00000513639.1:p.Pro150Ala
ENST00000698269.1:c.*14C>G	ENSP00000513640.1:n.*14C>G
ENST00000698270.1:c.428-932C>G	ENSP00000513641.1:n.428-932C>G
ENST00000698271.1:c.448C>G	ENSP00000513642.1:p.Pro150Ala
ENST00000698272.1:c.448C>G	ENSP00000513643.1:p.Pro150Ala
ENST00000698273.1:c.439C>G	ENSP00000513644.1:p.Pro147Ala