Canonical Allele Identifier: CA1785887865

Gene: PLAG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.56183310G= , CM000670.2:g.56183310G=	GRCh38
NC_000008.10:g.57095869G= , CM000670.1:g.57095869G=	GRCh37
NC_000008.9:g.57258423G=	NCBI36
NG_023310.1:g.32991C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000316981.8:c.-321-3797C= MANE Select	ENSP00000325546.3:n.-321-3797C=
ENST00000316981.7:c.-321-3797C=	ENSP00000325546.3:n.-321-3797C=
ENST00000423799.6:c.-103-12121C=	ENSP00000404067.2:n.-103-12121C=
ENST00000429357.2:c.-216-12121C=	ENSP00000416537.2:n.-216-12121C=
NM_001114634.1:c.-216-12121C=	NP_001108106.1:n.-216-12121C=
NM_001114635.1:c.-103-12121C=	NP_001108107.1:n.-103-12121C=
NM_002655.2:c.-321-3797C=	NP_002646.2:n.-321-3797C=
XM_011517544.1:c.-253-12121C=	XP_011515846.1:n.-253-12121C=
XM_011517544.2:c.-253-12121C=	XP_011515846.1:n.-253-12121C=
XM_017013576.1:c.-449-3797C=	XP_016869065.1:n.-449-3797C=
XM_017013577.1:c.-208-3797C=	XP_016869066.1:n.-208-3797C=
NM_002655.3:c.-321-3797C= MANE Select	NP_002646.2:n.-321-3797C=
NM_001114634.2:c.-216-12121C=	NP_001108106.1:n.-216-12121C=
NM_001114635.2:c.-103-12121C=	NP_001108107.1:n.-103-12121C=