Canonical Allele Identifier: CA2521826124
Gene: PLAG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.56183214A>T , CM000670.2:g.56183214A>T GRCh38
NC_000008.10:g.57095773A>T , CM000670.1:g.57095773A>T GRCh37
NC_000008.9:g.57258327A>T NCBI36
NG_023310.1:g.33087T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316981.8:c.-321-3701T>A MANE Select ENSP00000325546.3:n.-321-3701T>A
ENST00000316981.7:c.-321-3701T>A ENSP00000325546.3:n.-321-3701T>A
ENST00000423799.6:c.-103-12025T>A ENSP00000404067.2:n.-103-12025T>A
ENST00000429357.2:c.-216-12025T>A ENSP00000416537.2:n.-216-12025T>A
NM_001114634.1:c.-216-12025T>A NP_001108106.1:n.-216-12025T>A
NM_001114635.1:c.-103-12025T>A NP_001108107.1:n.-103-12025T>A
NM_002655.2:c.-321-3701T>A NP_002646.2:n.-321-3701T>A
XM_011517544.1:c.-253-12025T>A XP_011515846.1:n.-253-12025T>A
XM_011517544.2:c.-253-12025T>A XP_011515846.1:n.-253-12025T>A
XM_017013576.1:c.-449-3701T>A XP_016869065.1:n.-449-3701T>A
XM_017013577.1:c.-208-3701T>A XP_016869066.1:n.-208-3701T>A
NM_002655.3:c.-321-3701T>A MANE Select NP_002646.2:n.-321-3701T>A
NM_001114634.2:c.-216-12025T>A NP_001108106.1:n.-216-12025T>A
NM_001114635.2:c.-103-12025T>A NP_001108107.1:n.-103-12025T>A