Canonical Allele Identifier: CA2259186167

Gene: PPP1R1B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39634676G= , CM000679.2:g.39634676G=	GRCh38
NC_000017.10:g.37790929G= , CM000679.1:g.37790929G=	GRCh37
NC_000017.9:g.35044455G=	NCBI36
NG_030330.1:g.12753G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254079.9:c.445+590G= MANE Select	ENSP00000254079.4:n.445+590G=
ENST00000254079.8:c.445+590G=	ENSP00000254079.4:n.445+590G=
ENST00000394265.5:c.337+590G=	ENSP00000377808.1:n.337+590G=
ENST00000394267.2:c.337+590G=	ENSP00000377810.2:n.337+590G=
ENST00000492037.5:n.362+590G=
ENST00000579000.5:c.346+590G=	ENSP00000462841.1:n.346+590G=
ENST00000580029.1:n.1949+590G=
ENST00000580825.5:c.445+590G=	ENSP00000462137.1:n.445+590G=
ENST00000583446.5:n.469+590G=
NM_001242464.1:c.337+590G=	NP_001229393.1:n.337+590G=
NM_032192.3:c.445+590G=	NP_115568.2:n.445+590G=
NM_181505.3:c.337+590G=	NP_852606.1:n.337+590G=
XM_006722137.2:c.445+590G=	XP_006722200.1:n.445+590G=
XM_017025216.2:c.445+590G=	XP_016880705.1:n.445+590G=
XM_017025217.2:c.337+590G=	XP_016880706.1:n.337+590G=
NM_032192.4:c.445+590G= MANE Select	NP_115568.2:n.445+590G=
NM_001242464.2:c.337+590G=	NP_001229393.1:n.337+590G=
NM_181505.4:c.337+590G=	NP_852606.1:n.337+590G=