Canonical Allele Identifier: CA406758455
Gene: PPP1R15A HGNC NCBI

Linked Data

dbSNP Id: rs1430975128
gnomAD v2: 19-49379069-C-A
gnomAD v4: 19-48875812-C-A
MyVariant Identifiers: chr19:g.49379069C>A (hg19) chr19:g.48875812C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48875812C>A , CM000681.2:g.48875812C>A GRCh38
NC_000019.9:g.49379069C>A , CM000681.1:g.49379069C>A GRCh37
NC_000019.8:g.54070881C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000600406.2:c.*719C>A ENSP00000469239.2:n.*719C>A
ENST00000704026.1:c.1579C>A ENSP00000515636.1:p.Pro527Thr
ENST00000704027.1:c.1912C>A ENSP00000515637.1:p.Pro638Thr
ENST00000200453.6:c.1864C>A MANE Select ENSP00000200453.4:p.Pro622Thr
ENST00000200453.5:c.1864C>A ENSP00000200453.4:p.Pro622Thr
ENST00000600406.1:c.1495C>A
NM_014330.3:c.1864C>A NP_055145.3:p.Pro622Thr
NM_014330.5:c.1864C>A MANE Select NP_055145.3:p.Pro622Thr
Search 100 bp 5'
Search 100 bp 3'