Canonical Allele Identifier: CA1978928459
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64758509G= , CM000673.2:g.64758509G= GRCh38
NC_000011.9:g.64525981G= , CM000673.1:g.64525981G= GRCh37
NC_000011.8:g.64282557G= NCBI36
NG_013018.1:g.7207C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.352C= MANE Select ENSP00000164139.3:p.Leu118=
ENST00000164139.3:c.352C= ENSP00000164139.3:p.Leu118=
ENST00000377432.7:c.244-243C= ENSP00000366650.3:n.244-243C=
NM_001164716.1:c.244-243C= NP_001158188.1:n.244-243C=
NM_005609.2:c.352C= NP_005600.1:p.Leu118=
NM_005609.3:c.352C= NP_005600.1:p.Leu118=
NM_005609.4:c.352C= MANE Select NP_005600.1:p.Leu118=