Canonical Allele Identifier: CA340643598
Gene: PGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63623612C>T , CM000663.2:g.63623612C>T GRCh38
NC_000001.10:g.64089283C>T , CM000663.1:g.64089283C>T GRCh37
NC_000001.9:g.63861871C>T NCBI36
NG_016966.1:g.35337C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.247-5813C>T MANE Select ENSP00000360125.3:n.247-5813C>T
ENST00000650546.1:c.247-5813C>T ENSP00000497812.1:n.247-5813C>T
ENST00000371083.4:c.152C>T ENSP00000360124.4:p.Pro51Leu
ENST00000371084.7:c.247-5813C>T ENSP00000360125.3:n.247-5813C>T
ENST00000540265.5:c.-345-5813C>T ENSP00000443449.1:n.-345-5813C>T
NM_001172818.1:c.152C>T NP_001166289.1:p.Pro51Leu
NM_001172819.1:c.-345-5813C>T NP_001166290.1:n.-345-5813C>T
NM_002633.2:c.247-5813C>T NP_002624.2:n.247-5813C>T
NM_002633.3:c.247-5813C>T MANE Select NP_002624.2:n.247-5813C>T
NM_001172819.2:c.-345-5813C>T NP_001166290.1:n.-345-5813C>T