Canonical Allele Identifier: CA1171570964
Gene: PGM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63629164C= , CM000663.2:g.63629164C= GRCh38
NC_000001.10:g.64094835C= , CM000663.1:g.64094835C= GRCh37
NC_000001.9:g.63867423C= NCBI36
NG_016966.1:g.40889C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.247-261C= MANE Select ENSP00000360125.3:n.247-261C=
ENST00000650546.1:c.247-261C= ENSP00000497812.1:n.247-261C=
ENST00000371083.4:c.301-261C= ENSP00000360124.4:n.301-261C=
ENST00000371084.7:c.247-261C= ENSP00000360125.3:n.247-261C=
ENST00000540265.5:c.-345-261C= ENSP00000443449.1:n.-345-261C=
NM_001172818.1:c.301-261C= NP_001166289.1:n.301-261C=
NM_001172819.1:c.-345-261C= NP_001166290.1:n.-345-261C=
NM_002633.2:c.247-261C= NP_002624.2:n.247-261C=
NM_002633.3:c.247-261C= MANE Select NP_002624.2:n.247-261C=
NM_001172819.2:c.-345-261C= NP_001166290.1:n.-345-261C=
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