Canonical Allele Identifier: CA1171571077
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63629437G= , CM000663.2:g.63629437G= GRCh38
NC_000001.10:g.64095108G= , CM000663.1:g.64095108G= GRCh37
NC_000001.9:g.63867696G= NCBI36
NG_016966.1:g.41162G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371084.8:c.259G= MANE Select ENSP00000360125.3:p.Val87=
ENST00000650546.1:c.259G= ENSP00000497812.1:p.Val87=
ENST00000371083.4:c.313G= ENSP00000360124.4:p.Val105=
ENST00000371084.7:c.259G= ENSP00000360125.3:p.Val87=
ENST00000540265.5:c.-333G= ENSP00000443449.1:n.-333G=
NM_001172818.1:c.313G= NP_001166289.1:p.Val105=
NM_001172819.1:c.-333G= NP_001166290.1:n.-333G=
NM_002633.2:c.259G= NP_002624.2:p.Val87=
NM_002633.3:c.259G= MANE Select NP_002624.2:p.Val87=
NM_001172819.2:c.-333G= NP_001166290.1:n.-333G=