Canonical Allele Identifier: CA2598628079
Gene: PLAG1 HGNC NCBI

Linked Data

dbSNP Id: rs1585797521
gnomAD v3: 8-56183071-T-A
gnomAD v4: 8-56183071-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.56183071T>A , CM000670.2:g.56183071T>A GRCh38
NC_000008.10:g.57095630T>A , CM000670.1:g.57095630T>A GRCh37
NC_000008.9:g.57258184T>A NCBI36
NG_023310.1:g.33230A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316981.8:c.-321-3558A>T MANE Select ENSP00000325546.3:n.-321-3558A>T
ENST00000316981.7:c.-321-3558A>T ENSP00000325546.3:n.-321-3558A>T
ENST00000423799.6:c.-103-11882A>T ENSP00000404067.2:n.-103-11882A>T
ENST00000429357.2:c.-216-11882A>T ENSP00000416537.2:n.-216-11882A>T
NM_001114634.1:c.-216-11882A>T NP_001108106.1:n.-216-11882A>T
NM_001114635.1:c.-103-11882A>T NP_001108107.1:n.-103-11882A>T
NM_002655.2:c.-321-3558A>T NP_002646.2:n.-321-3558A>T
XM_011517544.1:c.-253-11882A>T XP_011515846.1:n.-253-11882A>T
XM_011517544.2:c.-253-11882A>T XP_011515846.1:n.-253-11882A>T
XM_017013576.1:c.-449-3558A>T XP_016869065.1:n.-449-3558A>T
XM_017013577.1:c.-208-3558A>T XP_016869066.1:n.-208-3558A>T
NM_002655.3:c.-321-3558A>T MANE Select NP_002646.2:n.-321-3558A>T
NM_001114634.2:c.-216-11882A>T NP_001108106.1:n.-216-11882A>T
NM_001114635.2:c.-103-11882A>T NP_001108107.1:n.-103-11882A>T