Canonical Allele Identifier: CA1785911663

Gene: PLAG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.56187590G= , CM000670.2:g.56187590G=	GRCh38
NC_000008.10:g.57100149G= , CM000670.1:g.57100149G=	GRCh37
NC_000008.9:g.57262703G=	NCBI36
NG_023310.1:g.28711C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316981.8:c.-321-8077C= MANE Select	ENSP00000325546.3:n.-321-8077C=
ENST00000316981.7:c.-321-8077C=	ENSP00000325546.3:n.-321-8077C=
ENST00000423799.6:c.-103-16401C=	ENSP00000404067.2:n.-103-16401C=
ENST00000429357.2:c.-216-16401C=	ENSP00000416537.2:n.-216-16401C=
NM_001114634.1:c.-216-16401C=	NP_001108106.1:n.-216-16401C=
NM_001114635.1:c.-103-16401C=	NP_001108107.1:n.-103-16401C=
NM_002655.2:c.-321-8077C=	NP_002646.2:n.-321-8077C=
XM_011517544.1:c.-253-16401C=	XP_011515846.1:n.-253-16401C=
XM_011517544.2:c.-253-16401C=	XP_011515846.1:n.-253-16401C=
XM_017013576.1:c.-449-8077C=	XP_016869065.1:n.-449-8077C=
XM_017013577.1:c.-208-8077C=	XP_016869066.1:n.-208-8077C=
NM_002655.3:c.-321-8077C= MANE Select	NP_002646.2:n.-321-8077C=
NM_001114634.2:c.-216-16401C=	NP_001108106.1:n.-216-16401C=
NM_001114635.2:c.-103-16401C=	NP_001108107.1:n.-103-16401C=