Canonical Allele Identifier: CA508078130

Gene: PPP1R15A

Linked Data

• MyVariant Identifiers: chr19:g.49379071A>T (hg19)

Genomic Alleles

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

Transcript Alleles

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