Canonical Allele Identifier: CA340635358
Community Standard Title: NM_002633.3(PGM1):c.878G>A (p.Arg293Gln)
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63636238G>A , CM000663.2:g.63636238G>A GRCh38
NC_000001.10:g.64101909G>A , CM000663.1:g.64101909G>A GRCh37
NC_000001.9:g.63874497G>A NCBI36
NG_016966.1:g.47963G>A

Transcript Alleles

HGVS Amino-acid Change
NM_002633.3:c.878G>A MANE Select NP_002624.2:p.Arg293Gln
ENST00000371084.8:c.878G>A MANE Select ENSP00000360125.3:p.Arg293Gln
NM_001172818.1:c.932G>A NP_001166289.1:p.Arg311Gln
NM_001172819.1:c.287G>A NP_001166290.1:p.Arg96Gln
NM_001172819.2:c.287G>A NP_001166290.1:p.Arg96Gln
NM_002633.2:c.878G>A NP_002624.2:p.Arg293Gln
ENST00000371083.4:c.932G>A ENSP00000360124.4:p.Arg311Gln
ENST00000371084.7:c.878G>A ENSP00000360125.3:p.Arg293Gln
ENST00000540265.5:c.287G>A ENSP00000443449.1:p.Arg96Gln
ENST00000650546.1:c.878G>A ENSP00000497812.1:p.Arg293Gln