Canonical Allele Identifier: CA1139772398

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30626965C= , CM000684.2:g.30626965C=	GRCh38
NC_000022.10:g.31022952C= , CM000684.1:g.31022952C=	GRCh37
NC_000022.9:g.29352952C=	NCBI36
NG_007263.1:g.24792C= , LRG_116:g.24792C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.*444C= MANE Select	NP_000346.2:n.*444C=
ENST00000215838.8:c.*444C= MANE Select	ENSP00000215838.3:n.*444C=
NM_000355.3:c.*444C=	NP_000346.2:n.*444C=
NM_001184726.1:c.*444C=	NP_001171655.1:n.*444C=
NM_001184726.2:c.*444C=	NP_001171655.1:n.*444C=
ENST00000215838.7:c.*444C=	ENSP00000215838.3:n.*444C=
ENST00000405742.7:c.*444C=	ENSP00000385914.3:n.*444C=
ENST00000407817.3:c.*444C=	ENSP00000384914.3:n.*444C=
ENST00000450638.5:c.*444C=	ENSP00000394184.2:n.*444C=
ENST00000471659.2:n.3819C=
ENST00000698264.1:n.3464C=
ENST00000698265.1:c.*444C=	ENSP00000513636.1:n.*444C=
ENST00000698266.1:c.*554C=	ENSP00000513637.1:n.*554C=
ENST00000698267.1:c.*584C=	ENSP00000513638.1:n.*584C=
ENST00000698268.1:c.*444C=	ENSP00000513639.1:n.*444C=
ENST00000698269.1:c.*1294C=	ENSP00000513640.1:n.*1294C=
ENST00000698270.1:c.*444C=	ENSP00000513641.1:n.*444C=
ENST00000698271.1:c.*444C=	ENSP00000513642.1:n.*444C=
ENST00000698272.1:c.*444C=	ENSP00000513643.1:n.*444C=
ENST00000698273.1:c.*444C=	ENSP00000513644.1:n.*444C=