Canonical Allele Identifier: CA411211103

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30614502G>C , CM000684.2:g.30614502G>C	GRCh38
NC_000022.10:g.31010489G>C , CM000684.1:g.31010489G>C	GRCh37
NC_000022.9:g.29340489G>C	NCBI36
NG_007263.1:g.12329G>C , LRG_116:g.12329G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.580+1G>C MANE Select	NP_000346.2:n.580+1G>C
ENST00000215838.8:c.580+1G>C MANE Select	ENSP00000215838.3:n.580+1G>C
NM_000355.3:c.580+1G>C	NP_000346.2:n.580+1G>C
NM_001184726.1:c.499+1G>C	NP_001171655.1:n.499+1G>C
NM_001184726.2:c.499+1G>C	NP_001171655.1:n.499+1G>C
ENST00000215838.7:c.580+1G>C	ENSP00000215838.3:n.580+1G>C
ENST00000405742.7:c.568+1G>C	ENSP00000385914.3:n.568+1G>C
ENST00000407817.3:c.499+1G>C	ENSP00000384914.3:n.499+1G>C
ENST00000450638.5:c.505+1G>C	ENSP00000394184.2:n.505+1G>C
ENST00000471659.2:n.2057+1G>C
ENST00000698263.1:c.580+1G>C	ENSP00000513635.1:n.580+1G>C
ENST00000698264.1:n.2057+1G>C
ENST00000698265.1:c.580+1G>C	ENSP00000513636.1:n.580+1G>C
ENST00000698266.1:c.580+1G>C	ENSP00000513637.1:n.580+1G>C
ENST00000698267.1:c.580+1G>C	ENSP00000513638.1:n.580+1G>C
ENST00000698268.1:c.580+1G>C	ENSP00000513639.1:n.580+1G>C
ENST00000698269.1:c.*146+1G>C	ENSP00000513640.1:n.*146+1G>C
ENST00000698270.1:c.428-799G>C	ENSP00000513641.1:n.428-799G>C
ENST00000698271.1:c.580+1G>C	ENSP00000513642.1:n.580+1G>C
ENST00000698272.1:c.580+1G>C	ENSP00000513643.1:n.580+1G>C
ENST00000698273.1:c.571+1G>C	ENSP00000513644.1:n.571+1G>C