Canonical Allele Identifier: CA10184999

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30623010C>T , CM000684.2:g.30623010C>T	GRCh38
NC_000022.10:g.31018997C>T , CM000684.1:g.31018997C>T	GRCh37
NC_000022.9:g.29348997C>T	NCBI36
NG_007263.1:g.20837C>T , LRG_116:g.20837C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.1149C>T MANE Select	NP_000346.2:p.Ser383=
ENST00000215838.8:c.1149C>T MANE Select	ENSP00000215838.3:p.Ser383=
NM_000355.3:c.1149C>T	NP_000346.2:p.Ser383=
NM_001184726.1:c.1068C>T	NP_001171655.1:p.Ser356=
NM_001184726.2:c.1068C>T	NP_001171655.1:p.Ser356=
ENST00000215838.7:c.1149C>T	ENSP00000215838.3:p.Ser383=
ENST00000405742.7:c.1137C>T	ENSP00000385914.3:p.Ser379=
ENST00000407817.3:c.1068C>T	ENSP00000384914.3:p.Ser356=
ENST00000450638.5:c.1074C>T	ENSP00000394184.2:p.Ser358=
ENST00000471659.2:n.3240C>T
ENST00000493542.1:n.281C>T
ENST00000698263.1:c.1107-3450C>T	ENSP00000513635.1:n.1107-3450C>T
ENST00000698264.1:n.2885C>T
ENST00000698265.1:c.1134C>T	ENSP00000513636.1:p.Ser378=
ENST00000698266.1:c.1149C>T	ENSP00000513637.1:p.Ser383=
ENST00000698267.1:c.*5C>T	ENSP00000513638.1:n.*5C>T
ENST00000698268.1:c.1176C>T	ENSP00000513639.1:p.Ser392=
ENST00000698269.1:c.*715C>T	ENSP00000513640.1:n.*715C>T
ENST00000698270.1:c.996C>T	ENSP00000513641.1:p.Ser332=
ENST00000698271.1:c.1179C>T	ENSP00000513642.1:p.Ser393=
ENST00000698272.1:c.1140C>T	ENSP00000513643.1:p.Ser380=
ENST00000698273.1:c.1140C>T	ENSP00000513644.1:p.Ser380=