Canonical Allele Identifier: CA340638236
Gene: PGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63648541A>T , CM000663.2:g.63648541A>T GRCh38
NC_000001.10:g.64114212A>T , CM000663.1:g.64114212A>T GRCh37
NC_000001.9:g.63886800A>T NCBI36
NG_016966.1:g.60266A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371084.8:c.1169A>T MANE Select ENSP00000360125.3:p.Asp390Val
ENST00000650546.1:c.1169A>T ENSP00000497812.1:p.Asp390Val
ENST00000371083.4:c.1223A>T ENSP00000360124.4:p.Asp408Val
ENST00000371084.7:c.1169A>T ENSP00000360125.3:p.Asp390Val
ENST00000540265.5:c.578A>T ENSP00000443449.1:p.Asp193Val
NM_001172818.1:c.1223A>T NP_001166289.1:p.Asp408Val
NM_001172819.1:c.578A>T NP_001166290.1:p.Asp193Val
NM_002633.2:c.1169A>T NP_002624.2:p.Asp390Val
NM_002633.3:c.1169A>T MANE Select NP_002624.2:p.Asp390Val
NM_001172819.2:c.578A>T NP_001166290.1:p.Asp193Val