Canonical Allele Identifier: CA340646481

Gene: PGM1

Linked Data

• dbSNP Id: rs1306739280
• gnomAD v2: 1-64095258-G-A
• gnomAD v4: 1-63629587-G-A
• MyVariant Identifiers: chr1:g.64095258G>A (hg19) ; chr1:g.63629587G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63629587G>A , CM000663.2:g.63629587G>A	GRCh38
NC_000001.10:g.64095258G>A , CM000663.1:g.64095258G>A	GRCh37
NC_000001.9:g.63867846G>A	NCBI36
NG_016966.1:g.41312G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371084.8:c.409G>A MANE Select	ENSP00000360125.3:p.Gly137Ser
ENST00000650546.1:c.409G>A	ENSP00000497812.1:p.Gly137Ser
ENST00000371083.4:c.463G>A	ENSP00000360124.4:p.Gly155Ser
ENST00000371084.7:c.409G>A	ENSP00000360125.3:p.Gly137Ser
ENST00000540265.5:c.-183G>A	ENSP00000443449.1:n.-183G>A
NM_001172818.1:c.463G>A	NP_001166289.1:p.Gly155Ser
NM_001172819.1:c.-183G>A	NP_001166290.1:n.-183G>A
NM_002633.2:c.409G>A	NP_002624.2:p.Gly137Ser
NM_002633.3:c.409G>A MANE Select	NP_002624.2:p.Gly137Ser
NM_001172819.2:c.-183G>A	NP_001166290.1:n.-183G>A