Canonical Allele Identifier: CA1145819750
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63648532G= , CM000663.2:g.63648532G= GRCh38
NC_000001.10:g.64114203G= , CM000663.1:g.64114203G= GRCh37
NC_000001.9:g.63886791G= NCBI36
NG_016966.1:g.60257G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371084.8:c.1160G= MANE Select ENSP00000360125.3:p.Arg387=
ENST00000650546.1:c.1160G= ENSP00000497812.1:p.Arg387=
ENST00000371083.4:c.1214G= ENSP00000360124.4:p.Arg405=
ENST00000371084.7:c.1160G= ENSP00000360125.3:p.Arg387=
ENST00000540265.5:c.569G= ENSP00000443449.1:p.Arg190=
NM_001172818.1:c.1214G= NP_001166289.1:p.Arg405=
NM_001172819.1:c.569G= NP_001166290.1:p.Arg190=
NM_002633.2:c.1160G= NP_002624.2:p.Arg387=
NM_002633.3:c.1160G= MANE Select NP_002624.2:p.Arg387=
NM_001172819.2:c.569G= NP_001166290.1:p.Arg190=