Canonical Allele Identifier: CA23832915
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63630265G>A , CM000663.2:g.63630265G>A GRCh38
NC_000001.10:g.64095936G>A , CM000663.1:g.64095936G>A GRCh37
NC_000001.9:g.63868524G>A NCBI36
NG_016966.1:g.41990G>A

Transcript Alleles

HGVS Amino-acid Change
NM_002633.3:c.556+177G>A MANE Select NP_002624.2:n.556+177G>A
ENST00000371084.8:c.556+177G>A MANE Select ENSP00000360125.3:n.556+177G>A
NM_001172818.1:c.610+177G>A NP_001166289.1:n.610+177G>A
NM_001172819.1:c.-36+177G>A NP_001166290.1:n.-36+177G>A
NM_001172819.2:c.-36+177G>A NP_001166290.1:n.-36+177G>A
NM_002633.2:c.556+177G>A NP_002624.2:n.556+177G>A
ENST00000371083.4:c.610+177G>A ENSP00000360124.4:n.610+177G>A
ENST00000371084.7:c.556+177G>A ENSP00000360125.3:n.556+177G>A
ENST00000540265.5:c.-36+177G>A ENSP00000443449.1:n.-36+177G>A
ENST00000650546.1:c.556+177G>A ENSP00000497812.1:n.556+177G>A