Canonical Allele Identifier: CA10184869

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30615729C>T , CM000684.2:g.30615729C>T	GRCh38
NC_000022.10:g.31011716C>T , CM000684.1:g.31011716C>T	GRCh37
NC_000022.9:g.29341716C>T	NCBI36
NG_007263.1:g.13556C>T , LRG_116:g.13556C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.882C>T MANE Select	NP_000346.2:p.Pro294=
ENST00000215838.8:c.882C>T MANE Select	ENSP00000215838.3:p.Pro294=
NM_000355.3:c.882C>T	NP_000346.2:p.Pro294=
NM_001184726.1:c.801C>T	NP_001171655.1:p.Pro267=
NM_001184726.2:c.801C>T	NP_001171655.1:p.Pro267=
ENST00000215838.7:c.882C>T	ENSP00000215838.3:p.Pro294=
ENST00000405742.7:c.870C>T	ENSP00000385914.3:p.Pro290=
ENST00000407817.3:c.801C>T	ENSP00000384914.3:p.Pro267=
ENST00000450638.5:c.807C>T	ENSP00000394184.2:p.Pro269=
ENST00000471659.1:n.38C>T
ENST00000471659.2:n.2359C>T
ENST00000493542.1:n.14C>T
ENST00000698263.1:c.882C>T	ENSP00000513635.1:p.Pro294=
ENST00000698264.1:n.2359C>T
ENST00000698265.1:c.882C>T	ENSP00000513636.1:p.Pro294=
ENST00000698266.1:c.882C>T	ENSP00000513637.1:p.Pro294=
ENST00000698267.1:c.882C>T	ENSP00000513638.1:p.Pro294=
ENST00000698268.1:c.882C>T	ENSP00000513639.1:p.Pro294=
ENST00000698269.1:c.*448C>T	ENSP00000513640.1:n.*448C>T
ENST00000698270.1:c.729C>T	ENSP00000513641.1:p.Pro243=
ENST00000698271.1:c.912C>T	ENSP00000513642.1:p.Pro304=
ENST00000698272.1:c.873C>T	ENSP00000513643.1:p.Pro291=
ENST00000698273.1:c.873C>T	ENSP00000513644.1:p.Pro291=