Canonical Allele Identifier: CA2743892760
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63629543dup , CM000663.2:g.63629543dup GRCh38
NC_000001.10:g.64095214dup , CM000663.1:g.64095214dup GRCh37
NC_000001.9:g.63867802dup NCBI36
NG_016966.1:g.41268dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.365dup MANE Select ENSP00000360125.3:p.Asn124GlnfsTer12
ENST00000650546.1:c.365dup ENSP00000497812.1:p.Asn124GlnfsTer12
ENST00000371083.4:c.419dup ENSP00000360124.4:p.Asn142GlnfsTer12
ENST00000371084.7:c.365dup ENSP00000360125.3:p.Asn124GlnfsTer12
ENST00000540265.5:c.-227dup ENSP00000443449.1:n.-227dup
NM_001172818.1:c.419dup NP_001166289.1:p.Asn142GlnfsTer12
NM_001172819.1:c.-227dup NP_001166290.1:n.-227dup
NM_002633.2:c.365dup NP_002624.2:p.Asn124GlnfsTer12
NM_002633.3:c.365dup MANE Select NP_002624.2:p.Asn124GlnfsTer12
NM_001172819.2:c.-227dup NP_001166290.1:n.-227dup