Canonical Allele Identifier: CA2843127677
Gene: PLAG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.56183219T>C , CM000670.2:g.56183219T>C GRCh38
NC_000008.10:g.57095778T>C , CM000670.1:g.57095778T>C GRCh37
NC_000008.9:g.57258332T>C NCBI36
NG_023310.1:g.33082A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000316981.8:c.-321-3706A>G MANE Select ENSP00000325546.3:n.-321-3706A>G
ENST00000316981.7:c.-321-3706A>G ENSP00000325546.3:n.-321-3706A>G
ENST00000423799.6:c.-103-12030A>G ENSP00000404067.2:n.-103-12030A>G
ENST00000429357.2:c.-216-12030A>G ENSP00000416537.2:n.-216-12030A>G
NM_001114634.1:c.-216-12030A>G NP_001108106.1:n.-216-12030A>G
NM_001114635.1:c.-103-12030A>G NP_001108107.1:n.-103-12030A>G
NM_002655.2:c.-321-3706A>G NP_002646.2:n.-321-3706A>G
XM_011517544.1:c.-253-12030A>G XP_011515846.1:n.-253-12030A>G
XM_011517544.2:c.-253-12030A>G XP_011515846.1:n.-253-12030A>G
XM_017013576.1:c.-449-3706A>G XP_016869065.1:n.-449-3706A>G
XM_017013577.1:c.-208-3706A>G XP_016869066.1:n.-208-3706A>G
NM_002655.3:c.-321-3706A>G MANE Select NP_002646.2:n.-321-3706A>G
NM_001114634.2:c.-216-12030A>G NP_001108106.1:n.-216-12030A>G
NM_001114635.2:c.-103-12030A>G NP_001108107.1:n.-103-12030A>G