Canonical Allele Identifier: CA379711403
Gene: TEAD1 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.12937202T>A
GRCh37 chr11:g.12958749T>A
Revel Score:
ENST00000361905 0.863
ENST00000527636 (MANE Select) 0.863
ENST00000527575 0.863
ENST00000334310 0.863
ENST00000361985 0.863
ENST00000526600 0.863
ClinVar RCV:
RCV001264402
ClinVar Variation:
984436
dbSNP:
11567847
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000527575.6:c.1087T>A ENSP00000435977.2:p.Tyr363Asn
ENST00000527636.7:c.1261T>A MANE Select ENSP00000435233.2:p.Tyr421Asn
ENST00000334310.10:c.1054T>A ENSP00000334754.6:p.Tyr352Asn
ENST00000361985.6:c.1066T>A ENSP00000354588.3:p.Tyr356Asn
ENST00000526600.1:c.973T>A ENSP00000435393.1:p.Tyr325Asn
ENST00000527575.5:c.1087T>A ENSP00000435977.1:p.Tyr363Asn
ENST00000527636.5:c.1261T>A ENSP00000435233.1:p.Tyr421Asn
NM_021961.5:c.1261T>A NP_068780.2:p.Tyr421Asn
NM_021961.6:c.1261T>A MANE Select NP_068780.2:p.Tyr421Asn
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