Canonical Allele Identifier: CA381169262
Gene: PYGM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64751433T>C , CM000673.2:g.64751433T>C GRCh38
NC_000011.9:g.64518905T>C , CM000673.1:g.64518905T>C GRCh37
NC_000011.8:g.64275481T>C NCBI36
NG_013018.1:g.14283A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.1861A>G MANE Select ENSP00000164139.3:p.Ile621Val
ENST00000164139.3:c.1861A>G ENSP00000164139.3:p.Ile621Val
ENST00000377432.7:c.1597A>G ENSP00000366650.3:p.Ile533Val
ENST00000462303.1:n.185A>G
NM_001164716.1:c.1597A>G NP_001158188.1:p.Ile533Val
NM_005609.2:c.1861A>G NP_005600.1:p.Ile621Val
NM_005609.3:c.1861A>G NP_005600.1:p.Ile621Val
NM_005609.4:c.1861A>G MANE Select NP_005600.1:p.Ile621Val