Canonical Allele Identifier: CA381167634
Gene: PYGM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64750431T>C , CM000673.2:g.64750431T>C GRCh38
NC_000011.9:g.64517903T>C , CM000673.1:g.64517903T>C GRCh37
NC_000011.8:g.64274479T>C NCBI36
NG_007574.1:g.26A>G , LRG_100:g.26A>G
NG_013018.1:g.15285A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000164139.4:c.2122A>G MANE Select ENSP00000164139.3:p.Asn708Asp
ENST00000164139.3:c.2122A>G ENSP00000164139.3:p.Asn708Asp
ENST00000377432.7:c.1858A>G ENSP00000366650.3:p.Asn620Asp
NM_001164716.1:c.1858A>G NP_001158188.1:p.Asn620Asp
NM_005609.2:c.2122A>G NP_005600.1:p.Asn708Asp
NM_005609.3:c.2122A>G NP_005600.1:p.Asn708Asp
NM_005609.4:c.2122A>G MANE Select NP_005600.1:p.Asn708Asp