Canonical Allele Identifier: CA177671615

Gene: PLAG1

Linked Data

• dbSNP Id: rs994534573
• gnomAD v3: 8-56183316-C-T
• gnomAD v4: 8-56183316-C-T
• MyVariant Identifiers: chr8:g.57095875C>T (hg19) ; chr8:g.56183316C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.56183316C>T , CM000670.2:g.56183316C>T	GRCh38
NC_000008.10:g.57095875C>T , CM000670.1:g.57095875C>T	GRCh37
NC_000008.9:g.57258429C>T	NCBI36
NG_023310.1:g.32985G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316981.8:c.-321-3803G>A MANE Select	ENSP00000325546.3:n.-321-3803G>A
ENST00000316981.7:c.-321-3803G>A	ENSP00000325546.3:n.-321-3803G>A
ENST00000423799.6:c.-103-12127G>A	ENSP00000404067.2:n.-103-12127G>A
ENST00000429357.2:c.-216-12127G>A	ENSP00000416537.2:n.-216-12127G>A
NM_001114634.1:c.-216-12127G>A	NP_001108106.1:n.-216-12127G>A
NM_001114635.1:c.-103-12127G>A	NP_001108107.1:n.-103-12127G>A
NM_002655.2:c.-321-3803G>A	NP_002646.2:n.-321-3803G>A
XM_011517544.1:c.-253-12127G>A	XP_011515846.1:n.-253-12127G>A
XM_011517544.2:c.-253-12127G>A	XP_011515846.1:n.-253-12127G>A
XM_017013576.1:c.-449-3803G>A	XP_016869065.1:n.-449-3803G>A
XM_017013577.1:c.-208-3803G>A	XP_016869066.1:n.-208-3803G>A
NM_002655.3:c.-321-3803G>A MANE Select	NP_002646.2:n.-321-3803G>A
NM_001114634.2:c.-216-12127G>A	NP_001108106.1:n.-216-12127G>A
NM_001114635.2:c.-103-12127G>A	NP_001108107.1:n.-103-12127G>A