Canonical Allele Identifier: CA418208213

Gene: PGM1

Linked Data

• MyVariant Identifiers: chr1:g.64095257A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63629586A>G , CM000663.2:g.63629586A>G	GRCh38
NC_000001.10:g.64095257A>G , CM000663.1:g.64095257A>G	GRCh37
NC_000001.9:g.63867845A>G	NCBI36
NG_016966.1:g.41311A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371084.8:c.408A>G MANE Select	ENSP00000360125.3:p.Gly136=
ENST00000650546.1:c.408A>G	ENSP00000497812.1:p.Gly136=
ENST00000371083.4:c.462A>G	ENSP00000360124.4:p.Gly154=
ENST00000371084.7:c.408A>G	ENSP00000360125.3:p.Gly136=
ENST00000540265.5:c.-184A>G	ENSP00000443449.1:n.-184A>G
NM_001172818.1:c.462A>G	NP_001166289.1:p.Gly154=
NM_001172819.1:c.-184A>G	NP_001166290.1:n.-184A>G
NM_002633.2:c.408A>G	NP_002624.2:p.Gly136=
NM_002633.3:c.408A>G MANE Select	NP_002624.2:p.Gly136=
NM_001172819.2:c.-184A>G	NP_001166290.1:n.-184A>G