Canonical Allele Identifier: CA2401110085

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30613044T= , CM000684.2:g.30613044T=	GRCh38
NC_000022.10:g.31009031T= , CM000684.1:g.31009031T=	GRCh37
NC_000022.9:g.29339031T=	NCBI36
NG_007263.1:g.10871T= , LRG_116:g.10871T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.427+2T= MANE Select	NP_000346.2:n.427+2T=
ENST00000215838.8:c.427+2T= MANE Select	ENSP00000215838.3:n.427+2T=
NM_000355.3:c.427+2T=	NP_000346.2:n.427+2T=
NM_001184726.1:c.346+83T=	NP_001171655.1:n.346+83T=
NM_001184726.2:c.346+83T=	NP_001171655.1:n.346+83T=
ENST00000215838.7:c.427+2T=	ENSP00000215838.3:n.427+2T=
ENST00000405742.7:c.415+2T=	ENSP00000385914.3:n.415+2T=
ENST00000407817.3:c.346+83T=	ENSP00000384914.3:n.346+83T=
ENST00000450638.5:c.352+2T=	ENSP00000394184.2:n.352+2T=
ENST00000471659.2:n.600T=
ENST00000698263.1:c.427+2T=	ENSP00000513635.1:n.427+2T=
ENST00000698264.1:n.600T=
ENST00000698265.1:c.427+2T=	ENSP00000513636.1:n.427+2T=
ENST00000698266.1:c.427+2T=	ENSP00000513637.1:n.427+2T=
ENST00000698267.1:c.427+2T=	ENSP00000513638.1:n.427+2T=
ENST00000698268.1:c.427+2T=	ENSP00000513639.1:n.427+2T=
ENST00000698269.1:c.258-1305T=	ENSP00000513640.1:n.258-1305T=
ENST00000698270.1:c.427+2T=	ENSP00000513641.1:n.427+2T=
ENST00000698271.1:c.427+2T=	ENSP00000513642.1:n.427+2T=
ENST00000698272.1:c.427+2T=	ENSP00000513643.1:n.427+2T=
ENST00000698273.1:c.418+2T=	ENSP00000513644.1:n.418+2T=