Canonical Allele Identifier: CA1785887580

Gene: PLAG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.56183058A= , CM000670.2:g.56183058A=	GRCh38
NC_000008.10:g.57095617A= , CM000670.1:g.57095617A=	GRCh37
NC_000008.9:g.57258171A=	NCBI36
NG_023310.1:g.33243T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316981.8:c.-321-3545T= MANE Select	ENSP00000325546.3:n.-321-3545T=
ENST00000316981.7:c.-321-3545T=	ENSP00000325546.3:n.-321-3545T=
ENST00000423799.6:c.-103-11869T=	ENSP00000404067.2:n.-103-11869T=
ENST00000429357.2:c.-216-11869T=	ENSP00000416537.2:n.-216-11869T=
NM_001114634.1:c.-216-11869T=	NP_001108106.1:n.-216-11869T=
NM_001114635.1:c.-103-11869T=	NP_001108107.1:n.-103-11869T=
NM_002655.2:c.-321-3545T=	NP_002646.2:n.-321-3545T=
XM_011517544.1:c.-253-11869T=	XP_011515846.1:n.-253-11869T=
XM_011517544.2:c.-253-11869T=	XP_011515846.1:n.-253-11869T=
XM_017013576.1:c.-449-3545T=	XP_016869065.1:n.-449-3545T=
XM_017013577.1:c.-208-3545T=	XP_016869066.1:n.-208-3545T=
NM_002655.3:c.-321-3545T= MANE Select	NP_002646.2:n.-321-3545T=
NM_001114634.2:c.-216-11869T=	NP_001108106.1:n.-216-11869T=
NM_001114635.2:c.-103-11869T=	NP_001108107.1:n.-103-11869T=