Canonical Allele Identifier: CA340638465
Gene: PGM1 HGNC NCBI

Linked Data

gnomAD v4: 1-63648643-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63648643T>G , CM000663.2:g.63648643T>G GRCh38
NC_000001.10:g.64114314T>G , CM000663.1:g.64114314T>G GRCh37
NC_000001.9:g.63886902T>G NCBI36
NG_016966.1:g.60368T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371084.8:c.1271T>G MANE Select ENSP00000360125.3:p.Phe424Cys
ENST00000650546.1:c.1271T>G ENSP00000497812.1:p.Phe424Cys
ENST00000371083.4:c.1325T>G ENSP00000360124.4:p.Phe442Cys
ENST00000371084.7:c.1271T>G ENSP00000360125.3:p.Phe424Cys
ENST00000540265.5:c.680T>G ENSP00000443449.1:p.Phe227Cys
NM_001172818.1:c.1325T>G NP_001166289.1:p.Phe442Cys
NM_001172819.1:c.680T>G NP_001166290.1:p.Phe227Cys
NM_002633.2:c.1271T>G NP_002624.2:p.Phe424Cys
NM_002633.3:c.1271T>G MANE Select NP_002624.2:p.Phe424Cys
NM_001172819.2:c.680T>G NP_001166290.1:p.Phe227Cys