Canonical Allele Identifier: CA340638444
Gene: PGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63648633G>C , CM000663.2:g.63648633G>C GRCh38
NC_000001.10:g.64114304G>C , CM000663.1:g.64114304G>C GRCh37
NC_000001.9:g.63886892G>C NCBI36
NG_016966.1:g.60358G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371084.8:c.1261G>C MANE Select ENSP00000360125.3:p.Gly421Arg
ENST00000650546.1:c.1261G>C ENSP00000497812.1:p.Gly421Arg
ENST00000371083.4:c.1315G>C ENSP00000360124.4:p.Gly439Arg
ENST00000371084.7:c.1261G>C ENSP00000360125.3:p.Gly421Arg
ENST00000540265.5:c.670G>C ENSP00000443449.1:p.Gly224Arg
NM_001172818.1:c.1315G>C NP_001166289.1:p.Gly439Arg
NM_001172819.1:c.670G>C NP_001166290.1:p.Gly224Arg
NM_002633.2:c.1261G>C NP_002624.2:p.Gly421Arg
NM_002633.3:c.1261G>C MANE Select NP_002624.2:p.Gly421Arg
NM_001172819.2:c.670G>C NP_001166290.1:p.Gly224Arg