Canonical Allele Identifier: CA1978929868
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759748_64759770delinsCTCGTGGGGTGGCCACATTGCGG , CM000673.2:g.64759748_64759770delinsCTCGTGGGGTGGCCACATTGCGG GRCh38
NC_000011.9:g.64527220_64527242delinsCTCGTGGGGTGGCCACATTGCGG , CM000673.1:g.64527220_64527242delinsCTCGTGGGGTGGCCACATTGCGG GRCh37
NC_000011.8:g.64283796_64283818delinsCTCGTGGGGTGGCCACATTGCGG NCBI36
NG_013018.1:g.5946_5968delinsCCGCAATGTGGCCACCCCACGAG

Transcript Alleles

HGVS Amino-acid change
ENST00000164139.4:c.129_151delinsCCGCAATGTGGCCACCCCACGAG MANE Select ENSP00000164139.3:p.Asp43=
ENST00000164139.3:c.129_151delinsCCGCAATGTGGCCACCCCACGAG ENSP00000164139.3:p.Asp43=
ENST00000377432.7:c.129_151delinsCCGCAATGTGGCCACCCCACGAG ENSP00000366650.3:p.Asp43=
NM_001164716.1:c.129_151delinsCCGCAATGTGGCCACCCCACGAG NP_001158188.1:p.Asp43=
NM_005609.2:c.129_151delinsCCGCAATGTGGCCACCCCACGAG NP_005600.1:p.Asp43=
NM_005609.3:c.129_151delinsCCGCAATGTGGCCACCCCACGAG NP_005600.1:p.Asp43=
NM_005609.4:c.129_151delinsCCGCAATGTGGCCACCCCACGAG MANE Select NP_005600.1:p.Asp43=