Canonical Allele Identifier: CA406758478
Gene: PPP1R15A HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49379079C>G (hg19) chr19:g.48875822C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48875822C>G , CM000681.2:g.48875822C>G GRCh38
NC_000019.9:g.49379079C>G , CM000681.1:g.49379079C>G GRCh37
NC_000019.8:g.54070891C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000600406.2:c.*729C>G ENSP00000469239.2:n.*729C>G
ENST00000704026.1:c.1589C>G ENSP00000515636.1:p.Ala530Gly
ENST00000704027.1:c.1922C>G ENSP00000515637.1:p.Ala641Gly
ENST00000200453.6:c.1874C>G MANE Select ENSP00000200453.4:p.Ala625Gly
ENST00000200453.5:c.1874C>G ENSP00000200453.4:p.Ala625Gly
ENST00000600406.1:c.1505C>G
NM_014330.3:c.1874C>G NP_055145.3:p.Ala625Gly
NM_014330.5:c.1874C>G MANE Select NP_055145.3:p.Ala625Gly
Search 100 bp 5'
Search 100 bp 3'