Canonical Allele Identifier: CA752351808

Gene: TCN2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30617488_30617490del , CM000684.2:g.30617488_30617490del	GRCh38
NC_000022.10:g.31013475_31013477del , CM000684.1:g.31013475_31013477del	GRCh37
NC_000022.9:g.29343475_29343477del	NCBI36
NG_007263.1:g.15315_15317del , LRG_116:g.15315_15317del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471659.2:n.2576_2578del
ENST00000698263.1:c.1099_1101del	ENSP00000513635.1:p.Gly367del
ENST00000698264.1:n.2576_2578del
ENST00000698265.1:c.1091+8_1091+10del	ENSP00000513636.1:n.1091+8_1091+10del
ENST00000698266.1:c.1099_1101del	ENSP00000513637.1:p.Gly367del
ENST00000698267.1:c.940+1701_940+1703del	ENSP00000513638.1:n.940+1701_940+1703del
ENST00000698268.1:c.1126_1128del	ENSP00000513639.1:p.Gly376del
ENST00000698269.1:c.*665_*667del	ENSP00000513640.1:n.*665_*667del
ENST00000698270.1:c.946_948del	ENSP00000513641.1:p.Gly316del
ENST00000698271.1:c.1129_1131del	ENSP00000513642.1:p.Gly377del
ENST00000698272.1:c.1090_1092del	ENSP00000513643.1:p.Gly364del
ENST00000698273.1:c.1090_1092del	ENSP00000513644.1:p.Gly364del
ENST00000215838.8:c.1099_1101del MANE Select	ENSP00000215838.3:p.Gly367del
ENST00000215838.7:c.1099_1101del	ENSP00000215838.3:p.Gly367del
ENST00000405742.7:c.1087_1089del	ENSP00000385914.3:p.Gly363del
ENST00000407817.3:c.1018_1020del	ENSP00000384914.3:p.Gly340del
ENST00000450638.5:c.1024_1026del	ENSP00000394184.2:p.Gly342del
ENST00000471659.1:n.255_257del
ENST00000493542.1:n.231_233del
NM_000355.3:c.1099_1101del	NP_000346.2:p.Gly367del
NM_001184726.1:c.1018_1020del	NP_001171655.1:p.Gly340del
NM_000355.4:c.1099_1101del MANE Select	NP_000346.2:p.Gly367del
NM_001184726.2:c.1018_1020del	NP_001171655.1:p.Gly340del