Canonical Allele Identifier: CA371379477

Gene: PLAG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.56168202C>T , CM000670.2:g.56168202C>T	GRCh38
NC_000008.10:g.57080761C>T , CM000670.1:g.57080761C>T	GRCh37
NC_000008.9:g.57243315C>T	NCBI36
NG_023310.1:g.48099G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316981.8:c.68G>A MANE Select	ENSP00000325546.3:p.Arg23His
ENST00000316981.7:c.68G>A	ENSP00000325546.3:p.Arg23His
ENST00000423799.6:c.-4-699G>A	ENSP00000404067.2:n.-4-699G>A
ENST00000429357.2:c.68G>A	ENSP00000416537.2:p.Arg23His
ENST00000522009.1:n.519G>A
NM_001114634.1:c.68G>A	NP_001108106.1:p.Arg23His
NM_001114635.1:c.-4-699G>A	NP_001108107.1:n.-4-699G>A
NM_002655.2:c.68G>A	NP_002646.2:p.Arg23His
XM_005251260.2:c.68G>A	XP_005251317.1:p.Arg23His
XM_011517544.1:c.-5+35G>A	XP_011515846.1:n.-5+35G>A
XM_011517544.2:c.-5+35G>A	XP_011515846.1:n.-5+35G>A
XM_017013576.1:c.68G>A	XP_016869065.1:p.Arg23His
XM_017013577.1:c.-4-699G>A	XP_016869066.1:n.-4-699G>A
NM_002655.3:c.68G>A MANE Select	NP_002646.2:p.Arg23His
NM_001114634.2:c.68G>A	NP_001108106.1:p.Arg23His
NM_001114635.2:c.-4-699G>A	NP_001108107.1:n.-4-699G>A