Canonical Allele Identifier: CA508078162

Gene: PPP1R15A

Linked Data

• MyVariant Identifiers: chr19:g.49379077A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48875820A>G , CM000681.2:g.48875820A>G	GRCh38
NC_000019.9:g.49379077A>G , CM000681.1:g.49379077A>G	GRCh37
NC_000019.8:g.54070889A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600406.2:c.*727A>G	ENSP00000469239.2:n.*727A>G
ENST00000704026.1:c.1587A>G	ENSP00000515636.1:p.Leu529=
ENST00000704027.1:c.1920A>G	ENSP00000515637.1:p.Leu640=
ENST00000200453.6:c.1872A>G MANE Select	ENSP00000200453.4:p.Leu624=
ENST00000200453.5:c.1872A>G	ENSP00000200453.4:p.Leu624=
ENST00000600406.1:c.1503A>G
NM_014330.3:c.1872A>G	NP_055145.3:p.Leu624=
NM_014330.5:c.1872A>G MANE Select	NP_055145.3:p.Leu624=