Canonical Allele Identifier: CA381167654
Gene: PYGM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64750434C>A , CM000673.2:g.64750434C>A GRCh38
NC_000011.9:g.64517906C>A , CM000673.1:g.64517906C>A GRCh37
NC_000011.8:g.64274482C>A NCBI36
NG_007574.1:g.23G>T , LRG_100:g.23G>T
NG_013018.1:g.15282G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.2119G>T MANE Select ENSP00000164139.3:p.Glu707Ter
ENST00000164139.3:c.2119G>T ENSP00000164139.3:p.Glu707Ter
ENST00000377432.7:c.1855G>T ENSP00000366650.3:p.Glu619Ter
NM_001164716.1:c.1855G>T NP_001158188.1:p.Glu619Ter
NM_005609.2:c.2119G>T NP_005600.1:p.Glu707Ter
NM_005609.3:c.2119G>T NP_005600.1:p.Glu707Ter
NM_005609.4:c.2119G>T MANE Select NP_005600.1:p.Glu707Ter