Canonical Allele Identifier: CA1252371306

Gene: PPP4R3B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55616277C= , CM000664.2:g.55616277C=	GRCh38
NC_000002.11:g.55843413C= , CM000664.1:g.55843413C=	GRCh37
NC_000002.10:g.55696917C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001122964.3:c.143-771G= MANE Select	NP_001116436.3:n.143-771G=
ENST00000616407.2:c.143-771G= MANE Select	ENSP00000483228.1:n.143-771G=
NM_001122964.2:c.143-771G=	NP_001116436.2:n.143-771G=
NM_001282850.1:c.143-771G=	NP_001269779.1:n.143-771G=
NM_001282850.2:c.143-771G=	NP_001269779.1:n.143-771G=
NM_020463.3:c.143-771G=	NP_065196.1:n.143-771G=
NM_020463.4:c.143-771G=	NP_065196.1:n.143-771G=
ENST00000470801.1:n.100+241G=
ENST00000611717.4:c.143-771G=	ENSP00000478677.1:n.143-771G=
ENST00000612688.1:n.1651-771G=
ENST00000616288.4:c.143-771G=	ENSP00000484116.1:n.143-771G=
ENST00000616407.1:c.143-771G=	ENSP00000483228.1:n.143-771G=
XM_005264442.2:c.143-771G=	XP_005264499.1:n.143-771G=
XM_005264442.3:c.143-771G=	XP_005264499.1:n.143-771G=
XM_005264444.2:c.143-771G=	XP_005264501.1:n.143-771G=
XM_005264444.3:c.143-771G=	XP_005264501.1:n.143-771G=
XM_005264445.2:c.143-771G=	XP_005264502.1:n.143-771G=
XM_005264445.3:c.143-771G=	XP_005264502.1:n.143-771G=
XM_005264446.2:c.143-771G=	XP_005264503.1:n.143-771G=
XM_005264446.3:c.143-771G=	XP_005264503.1:n.143-771G=
XM_005264447.2:c.143-771G=	XP_005264504.1:n.143-771G=
XM_005264447.3:c.143-771G=	XP_005264504.1:n.143-771G=
XM_011533002.1:c.143-771G=	XP_011531304.1:n.143-771G=
XM_017004531.2:c.143-771G=	XP_016860020.1:n.143-771G=
XM_017004532.2:c.143-771G=	XP_016860021.1:n.143-771G=
XM_017004533.2:c.143-771G=	XP_016860022.1:n.143-771G=
XM_017004534.2:c.143-771G=	XP_016860023.1:n.143-771G=
XM_017004535.2:c.143-771G=	XP_016860024.1:n.143-771G=
XM_017004536.2:c.143-771G=	XP_016860025.1:n.143-771G=
XM_017004537.2:c.-964-771G=	XP_016860026.1:n.-964-771G=
XM_017004538.2:c.-844-771G=	XP_016860027.1:n.-844-771G=
XM_017004539.2:c.-964-771G=	XP_016860028.1:n.-964-771G=
XM_017004540.2:c.-844-771G=	XP_016860029.1:n.-844-771G=
XM_024453014.1:c.143-771G=	XP_024308782.1:n.143-771G=
XR_001738855.2:n.559-771G=