Canonical Allele Identifier: CA122593

Gene: TEAD1

Linked Data

• ClinVar Variation Id: 12630
• ClinVar RCV Id: RCV000013465
• dbSNP Id: rs11567847
• MyVariant Identifiers: chr11:g.12958749T>C (hg19) ; chr11:g.12937202T>C (hg38)
• PubMed: PMID:15016762 ; PMID:17689488

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.12937202T>C , CM000673.2:g.12937202T>C	GRCh38
NC_000011.9:g.12958749T>C , CM000673.1:g.12958749T>C	GRCh37
NC_000011.8:g.12915325T>C	NCBI36
NG_021302.1:g.267781T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527575.6:c.1087T>C	ENSP00000435977.2:p.Tyr363His
ENST00000527636.7:c.1261T>C MANE Select	ENSP00000435233.2:p.Tyr421His
ENST00000334310.10:c.1054T>C	ENSP00000334754.6:p.Tyr352His
ENST00000361985.6:c.1066T>C	ENSP00000354588.3:p.Tyr356His
ENST00000526600.1:c.973T>C	ENSP00000435393.1:p.Tyr325His
ENST00000527575.5:c.1087T>C	ENSP00000435977.1:p.Tyr363His
ENST00000527636.5:c.1261T>C	ENSP00000435233.1:p.Tyr421His
NM_021961.5:c.1261T>C	NP_068780.2:p.Tyr421His
NM_021961.6:c.1261T>C MANE Select	NP_068780.2:p.Tyr421His