Canonical Allele Identifier: CA889780

Gene: PGM1

Linked Data

• ClinVar Variation Id: 285889
• ClinVar RCV Id: RCV000305843
• dbSNP Id: rs748019294
• ExAC: 1:64114307 C / T
• gnomAD v2: 1-64114307-C-T
• gnomAD v3: 1-63648636-C-T
• gnomAD v4: 1-63648636-C-T
• MyVariant Identifiers: chr1:g.64114307C>T (hg19) ; chr1:g.63648636C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63648636C>T , CM000663.2:g.63648636C>T	GRCh38
NC_000001.10:g.64114307C>T , CM000663.1:g.64114307C>T	GRCh37
NC_000001.9:g.63886895C>T	NCBI36
NG_016966.1:g.60361C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371084.8:c.1264C>T MANE Select	ENSP00000360125.3:p.Arg422Trp
ENST00000650546.1:c.1264C>T	ENSP00000497812.1:p.Arg422Trp
ENST00000371083.4:c.1318C>T	ENSP00000360124.4:p.Arg440Trp
ENST00000371084.7:c.1264C>T	ENSP00000360125.3:p.Arg422Trp
ENST00000540265.5:c.673C>T	ENSP00000443449.1:p.Arg225Trp
NM_001172818.1:c.1318C>T	NP_001166289.1:p.Arg440Trp
NM_001172819.1:c.673C>T	NP_001166290.1:p.Arg225Trp
NM_002633.2:c.1264C>T	NP_002624.2:p.Arg422Trp
NM_002633.3:c.1264C>T MANE Select	NP_002624.2:p.Arg422Trp
NM_001172819.2:c.673C>T	NP_001166290.1:p.Arg225Trp