Canonical Allele Identifier: CA508078128
Gene: PPP1R15A HGNC NCBI

Linked Data

gnomAD v4: 19-48875814-A-G
MyVariant Identifiers: chr19:g.49379071A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48875814A>G , CM000681.2:g.48875814A>G GRCh38
NC_000019.9:g.49379071A>G , CM000681.1:g.49379071A>G GRCh37
NC_000019.8:g.54070883A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000600406.2:c.*721A>G ENSP00000469239.2:n.*721A>G
ENST00000704026.1:c.1581A>G ENSP00000515636.1:p.Pro527=
ENST00000704027.1:c.1914A>G ENSP00000515637.1:p.Pro638=
ENST00000200453.6:c.1866A>G MANE Select ENSP00000200453.4:p.Pro622=
ENST00000200453.5:c.1866A>G ENSP00000200453.4:p.Pro622=
ENST00000600406.1:c.1497A>G
NM_014330.3:c.1866A>G NP_055145.3:p.Pro622=
NM_014330.5:c.1866A>G MANE Select NP_055145.3:p.Pro622=
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