Canonical Allele Identifier: CA497366659
Gene: PIEZO1 HGNC NCBI
HSALR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2179777
ClinVar RCV Id: RCV002615222
dbSNP Id: rs1904937786
gnomAD v3: 16-88732616-G-A
gnomAD v4: 16-88732616-G-A
COSMIC: COSM4636340
MyVariant Identifiers: chr16:g.88799024G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88732616G>A , CM000678.2:g.88732616G>A GRCh38
NC_000016.9:g.88799024G>A , CM000678.1:g.88799024G>A GRCh37
NC_000016.8:g.87326525G>A NCBI36
NG_042229.1:g.57605C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301015.14:c.2781C>T (PIEZO1) MANE Select ENSP00000301015.9:p.Gly927=
ENST00000301015.13:c.2781C>T (PIEZO1) ENSP00000301015.9:p.Gly927=
ENST00000490756.1:n.365C>T (PIEZO1)
NM_001142864.2:c.2781C>T (PIEZO1) NP_001136336.2:p.Gly927=
NM_001142864.3:c.2781C>T (PIEZO1) NP_001136336.2:p.Gly927=
NR_103774.1:n.269+1168G>A (HSALR1)
NM_001142864.4:c.2781C>T (PIEZO1) MANE Select NP_001136336.2:p.Gly927=
Search 100 bp 5'
Search 100 bp 3'