Canonical Allele Identifier: CA6080245
Gene: PYGM HGNC NCBI

Linked Data

dbSNP Id: rs779198403

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64758334G>A , CM000673.2:g.64758334G>A GRCh38
NC_000011.9:g.64525806G>A , CM000673.1:g.64525806G>A GRCh37
NC_000011.8:g.64282382G>A NCBI36
NG_013018.1:g.7382C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.440C>T MANE Select ENSP00000164139.3:p.Ser147Phe
ENST00000164139.3:c.440C>T ENSP00000164139.3:p.Ser147Phe
ENST00000377432.7:c.244-68C>T ENSP00000366650.3:n.244-68C>T
NM_001164716.1:c.244-68C>T NP_001158188.1:n.244-68C>T
NM_005609.2:c.440C>T NP_005600.1:p.Ser147Phe
NM_005609.3:c.440C>T NP_005600.1:p.Ser147Phe
NM_005609.4:c.440C>T MANE Select NP_005600.1:p.Ser147Phe