Canonical Allele Identifier: CA10651084

Gene: TCN2

Linked Data

• ClinVar Variation Id: 341226
• ClinVar RCV Id: RCV000339325
• dbSNP Id: rs10418
• gnomAD v2: 22-31022952-C-T
• gnomAD v3: 22-30626965-C-T
• gnomAD v4: 22-30626965-C-T
• MyVariant Identifiers: chr22:g.31022952C>T (hg19) ; chr22:g.30626965C>T (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

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

Transcript Alleles

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