Canonical Allele Identifier: CA1978930096
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759898T= , CM000673.2:g.64759898T= GRCh38
NC_000011.9:g.64527370T= , CM000673.1:g.64527370T= GRCh37
NC_000011.8:g.64283946T= NCBI36
NG_013018.1:g.5818A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.1A= MANE Select ENSP00000164139.3:p.Met1=
ENST00000164139.3:c.1A= ENSP00000164139.3:p.Met1=
ENST00000377432.7:c.1A= ENSP00000366650.3:p.Met1=
NM_001164716.1:c.1A= NP_001158188.1:p.Met1=
NM_005609.2:c.1A= NP_005600.1:p.Met1=
NM_005609.3:c.1A= NP_005600.1:p.Met1=
NM_005609.4:c.1A= MANE Select NP_005600.1:p.Met1=