Canonical Allele Identifier: CA4754894
Community Standard Title: NM_002655.3(PLAG1):c.589C>T (p.Arg197Ter)
Gene: PLAG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.56167157G>A , CM000670.2:g.56167157G>A GRCh38
NC_000008.10:g.57079716G>A , CM000670.1:g.57079716G>A GRCh37
NC_000008.9:g.57242270G>A NCBI36
NG_023310.1:g.49144C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002655.3:c.589C>T MANE Select NP_002646.2:p.Arg197Ter
ENST00000316981.8:c.589C>T MANE Select ENSP00000325546.3:p.Arg197Ter
NM_001114634.1:c.589C>T NP_001108106.1:p.Arg197Ter
NM_001114634.2:c.589C>T NP_001108106.1:p.Arg197Ter
NM_001114635.1:c.343C>T NP_001108107.1:p.Arg115Ter
NM_001114635.2:c.343C>T NP_001108107.1:p.Arg115Ter
NM_002655.2:c.589C>T NP_002646.2:p.Arg197Ter
ENST00000316981.7:c.589C>T ENSP00000325546.3:p.Arg197Ter
ENST00000423799.6:c.343C>T ENSP00000404067.2:p.Arg115Ter
ENST00000429357.2:c.589C>T ENSP00000416537.2:p.Arg197Ter
ENST00000522009.1:n.1040C>T
XM_005251260.2:c.589C>T XP_005251317.1:p.Arg197Ter
XM_011517544.1:c.343C>T XP_011515846.1:p.Arg115Ter
XM_011517544.2:c.343C>T XP_011515846.1:p.Arg115Ter
XM_017013576.1:c.589C>T XP_016869065.1:p.Arg197Ter
XM_017013577.1:c.343C>T XP_016869066.1:p.Arg115Ter