Canonical Allele Identifier: CA371376337

Gene: PLAG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.56166289A>C , CM000670.2:g.56166289A>C	GRCh38
NC_000008.10:g.57078848A>C , CM000670.1:g.57078848A>C	GRCh37
NC_000008.9:g.57241402A>C	NCBI36
NG_023310.1:g.50012T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316981.8:c.1457T>G MANE Select	ENSP00000325546.3:p.Leu486Ter
ENST00000316981.7:c.1457T>G	ENSP00000325546.3:p.Leu486Ter
ENST00000423799.6:c.1211T>G	ENSP00000404067.2:p.Leu404Ter
ENST00000429357.2:c.1457T>G	ENSP00000416537.2:p.Leu486Ter
ENST00000522009.1:n.1908T>G
NM_001114634.1:c.1457T>G	NP_001108106.1:p.Leu486Ter
NM_001114635.1:c.1211T>G	NP_001108107.1:p.Leu404Ter
NM_002655.2:c.1457T>G	NP_002646.2:p.Leu486Ter
XM_005251260.2:c.1457T>G	XP_005251317.1:p.Leu486Ter
XM_011517544.1:c.1211T>G	XP_011515846.1:p.Leu404Ter
XM_011517544.2:c.1211T>G	XP_011515846.1:p.Leu404Ter
XM_017013576.1:c.1457T>G	XP_016869065.1:p.Leu486Ter
XM_017013577.1:c.1211T>G	XP_016869066.1:p.Leu404Ter
NM_002655.3:c.1457T>G MANE Select	NP_002646.2:p.Leu486Ter
NM_001114634.2:c.1457T>G	NP_001108106.1:p.Leu486Ter
NM_001114635.2:c.1211T>G	NP_001108107.1:p.Leu404Ter