Canonical Allele Identifier: CA514220257

Gene: TCN2

Linked Data

• dbSNP Id: rs2087562918
• gnomAD v3: 22-30612951-C-G
• gnomAD v4: 22-30612951-C-G
• MyVariant Identifiers: chr22:g.31008938C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30612951C>G , CM000684.2:g.30612951C>G	GRCh38
NC_000022.10:g.31008938C>G , CM000684.1:g.31008938C>G	GRCh37
NC_000022.9:g.29338938C>G	NCBI36
NG_007263.1:g.10778C>G , LRG_116:g.10778C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471659.2:n.507C>G
ENST00000698263.1:c.336C>G	ENSP00000513635.1:p.Leu112=
ENST00000698264.1:n.507C>G
ENST00000698265.1:c.336C>G	ENSP00000513636.1:p.Leu112=
ENST00000698266.1:c.336C>G	ENSP00000513637.1:p.Leu112=
ENST00000698267.1:c.336C>G	ENSP00000513638.1:p.Leu112=
ENST00000698268.1:c.336C>G	ENSP00000513639.1:p.Leu112=
ENST00000698269.1:c.258-1398C>G	ENSP00000513640.1:n.258-1398C>G
ENST00000698270.1:c.336C>G	ENSP00000513641.1:p.Leu112=
ENST00000698271.1:c.336C>G	ENSP00000513642.1:p.Leu112=
ENST00000698272.1:c.336C>G	ENSP00000513643.1:p.Leu112=
ENST00000698273.1:c.327C>G	ENSP00000513644.1:p.Leu109=
ENST00000215838.8:c.336C>G MANE Select	ENSP00000215838.3:p.Leu112=
ENST00000215838.7:c.336C>G	ENSP00000215838.3:p.Leu112=
ENST00000405742.7:c.324C>G	ENSP00000385914.3:p.Leu108=
ENST00000407817.3:c.336C>G	ENSP00000384914.3:p.Leu112=
ENST00000450638.5:c.261C>G	ENSP00000394184.2:p.Leu87=
NM_000355.3:c.336C>G	NP_000346.2:p.Leu112=
NM_001184726.1:c.336C>G	NP_001171655.1:p.Leu112=
NM_000355.4:c.336C>G MANE Select	NP_000346.2:p.Leu112=
NM_001184726.2:c.336C>G	NP_001171655.1:p.Leu112=