Canonical Allele Identifier: CA9560462
Gene: PPP1R15A HGNC NCBI

Linked Data

dbSNP Id: rs35007147
ExAC: 19:49379177 C / T
gnomAD v2: 19-49379177-C-T
gnomAD v3: 19-48875920-C-T
gnomAD v4: 19-48875920-C-T
MyVariant Identifiers: chr19:g.49379177C>T (hg19) chr19:g.48875920C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48875920C>T , CM000681.2:g.48875920C>T GRCh38
NC_000019.9:g.49379177C>T , CM000681.1:g.49379177C>T GRCh37
NC_000019.8:g.54070989C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000600406.2:c.*827C>T ENSP00000469239.2:n.*827C>T
ENST00000704026.1:c.1687C>T ENSP00000515636.1:p.Arg563Cys
ENST00000704027.1:c.2020C>T ENSP00000515637.1:p.Arg674Cys
ENST00000200453.6:c.1972C>T MANE Select ENSP00000200453.4:p.Arg658Cys
ENST00000200453.5:c.1972C>T ENSP00000200453.4:p.Arg658Cys
ENST00000600406.1:c.1603C>T
NM_014330.3:c.1972C>T NP_055145.3:p.Arg658Cys
NM_014330.5:c.1972C>T MANE Select NP_055145.3:p.Arg658Cys
Search 100 bp 5'
Search 100 bp 3'