Canonical Allele Identifier: CA411216604

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30622978C>T , CM000684.2:g.30622978C>T	GRCh38
NC_000022.10:g.31018965C>T , CM000684.1:g.31018965C>T	GRCh37
NC_000022.9:g.29348965C>T	NCBI36
NG_007263.1:g.20805C>T , LRG_116:g.20805C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.1117C>T MANE Select	NP_000346.2:p.Gln373Ter
ENST00000215838.8:c.1117C>T MANE Select	ENSP00000215838.3:p.Gln373Ter
NM_000355.3:c.1117C>T	NP_000346.2:p.Gln373Ter
NM_001184726.1:c.1036C>T	NP_001171655.1:p.Gln346Ter
NM_001184726.2:c.1036C>T	NP_001171655.1:p.Gln346Ter
ENST00000215838.7:c.1117C>T	ENSP00000215838.3:p.Gln373Ter
ENST00000405742.7:c.1105C>T	ENSP00000385914.3:p.Gln369Ter
ENST00000407817.3:c.1036C>T	ENSP00000384914.3:p.Gln346Ter
ENST00000450638.5:c.1042C>T	ENSP00000394184.2:p.Gln348Ter
ENST00000471659.2:n.3208C>T
ENST00000493542.1:n.249C>T
ENST00000698263.1:c.1107-3482C>T	ENSP00000513635.1:n.1107-3482C>T
ENST00000698264.1:n.2853C>T
ENST00000698265.1:c.1102C>T	ENSP00000513636.1:p.Gln368Ter
ENST00000698266.1:c.1117C>T	ENSP00000513637.1:p.Gln373Ter
ENST00000698267.1:c.951C>T	ENSP00000513638.1:p.His317=
ENST00000698268.1:c.1144C>T	ENSP00000513639.1:p.Gln382Ter
ENST00000698269.1:c.*683C>T	ENSP00000513640.1:n.*683C>T
ENST00000698270.1:c.964C>T	ENSP00000513641.1:p.Gln322Ter
ENST00000698271.1:c.1147C>T	ENSP00000513642.1:p.Gln383Ter
ENST00000698272.1:c.1108C>T	ENSP00000513643.1:p.Gln370Ter
ENST00000698273.1:c.1108C>T	ENSP00000513644.1:p.Gln370Ter