Canonical Allele Identifier: CA1144032022
Gene: PGM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63629615G= , CM000663.2:g.63629615G= GRCh38
NC_000001.10:g.64095286G= , CM000663.1:g.64095286G= GRCh37
NC_000001.9:g.63867874G= NCBI36
NG_016966.1:g.41340G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.409+28G= MANE Select ENSP00000360125.3:n.409+28G=
ENST00000650546.1:c.409+28G= ENSP00000497812.1:n.409+28G=
ENST00000371083.4:c.463+28G= ENSP00000360124.4:n.463+28G=
ENST00000371084.7:c.409+28G= ENSP00000360125.3:n.409+28G=
ENST00000540265.5:c.-183+28G= ENSP00000443449.1:n.-183+28G=
NM_001172818.1:c.463+28G= NP_001166289.1:n.463+28G=
NM_001172819.1:c.-183+28G= NP_001166290.1:n.-183+28G=
NM_002633.2:c.409+28G= NP_002624.2:n.409+28G=
NM_002633.3:c.409+28G= MANE Select NP_002624.2:n.409+28G=
NM_001172819.2:c.-183+28G= NP_001166290.1:n.-183+28G=
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