Canonical Allele Identifier: CA340638439
Gene: PGM1 HGNC NCBI

Linked Data

gnomAD v4: 1-63648631-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63648631A>G , CM000663.2:g.63648631A>G GRCh38
NC_000001.10:g.64114302A>G , CM000663.1:g.64114302A>G GRCh37
NC_000001.9:g.63886890A>G NCBI36
NG_016966.1:g.60356A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371084.8:c.1259A>G MANE Select ENSP00000360125.3:p.Tyr420Cys
ENST00000650546.1:c.1259A>G ENSP00000497812.1:p.Tyr420Cys
ENST00000371083.4:c.1313A>G ENSP00000360124.4:p.Tyr438Cys
ENST00000371084.7:c.1259A>G ENSP00000360125.3:p.Tyr420Cys
ENST00000540265.5:c.668A>G ENSP00000443449.1:p.Tyr223Cys
NM_001172818.1:c.1313A>G NP_001166289.1:p.Tyr438Cys
NM_001172819.1:c.668A>G NP_001166290.1:p.Tyr223Cys
NM_002633.2:c.1259A>G NP_002624.2:p.Tyr420Cys
NM_002633.3:c.1259A>G MANE Select NP_002624.2:p.Tyr420Cys
NM_001172819.2:c.668A>G NP_001166290.1:p.Tyr223Cys