Canonical Allele Identifier: CA212722

Gene: TCN2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30615125A>T , CM000684.2:g.30615125A>T	GRCh38
NC_000022.10:g.31011112A>T , CM000684.1:g.31011112A>T	GRCh37
NC_000022.9:g.29341112A>T	NCBI36
NG_007263.1:g.12952A>T , LRG_116:g.12952A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471659.2:n.2058-176A>T
ENST00000698263.1:c.581-176A>T	ENSP00000513635.1:n.581-176A>T
ENST00000698264.1:n.2058-176A>T
ENST00000698265.1:c.581-176A>T	ENSP00000513636.1:n.581-176A>T
ENST00000698266.1:c.581-176A>T	ENSP00000513637.1:n.581-176A>T
ENST00000698267.1:c.581-176A>T	ENSP00000513638.1:n.581-176A>T
ENST00000698268.1:c.581-176A>T	ENSP00000513639.1:n.581-176A>T
ENST00000698269.1:c.*147-176A>T	ENSP00000513640.1:n.*147-176A>T
ENST00000698270.1:c.428-176A>T	ENSP00000513641.1:n.428-176A>T
ENST00000698271.1:c.581-146A>T	ENSP00000513642.1:n.581-146A>T
ENST00000698272.1:c.581-185A>T	ENSP00000513643.1:n.581-185A>T
ENST00000698273.1:c.572-176A>T	ENSP00000513644.1:n.572-176A>T
ENST00000215838.8:c.581-176A>T MANE Select	ENSP00000215838.3:n.581-176A>T
ENST00000215838.7:c.581-176A>T	ENSP00000215838.3:n.581-176A>T
ENST00000405742.7:c.569-176A>T	ENSP00000385914.3:n.569-176A>T
ENST00000407817.3:c.500-176A>T	ENSP00000384914.3:n.500-176A>T
ENST00000450638.5:c.506-176A>T	ENSP00000394184.2:n.506-176A>T
NM_000355.3:c.581-176A>T	NP_000346.2:n.581-176A>T
NM_001184726.1:c.500-176A>T	NP_001171655.1:n.500-176A>T
NM_000355.4:c.581-176A>T MANE Select	NP_000346.2:n.581-176A>T
NM_001184726.2:c.500-176A>T	NP_001171655.1:n.500-176A>T