Canonical Allele Identifier: CA889510
Community Standard Title: NM_002633.3(PGM1):c.327T>C (p.Ile109=)
Gene: PGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63629505T>C , CM000663.2:g.63629505T>C GRCh38
NC_000001.10:g.64095176T>C , CM000663.1:g.64095176T>C GRCh37
NC_000001.9:g.63867764T>C NCBI36
NG_016966.1:g.41230T>C

Transcript Alleles

HGVS Amino-acid Change
NM_002633.3:c.327T>C MANE Select NP_002624.2:p.Ile109=
ENST00000371084.8:c.327T>C MANE Select ENSP00000360125.3:p.Ile109=
NM_001172818.1:c.381T>C NP_001166289.1:p.Ile127=
NM_001172819.1:c.-265T>C NP_001166290.1:n.-265T>C
NM_001172819.2:c.-265T>C NP_001166290.1:n.-265T>C
NM_002633.2:c.327T>C NP_002624.2:p.Ile109=
ENST00000371083.4:c.381T>C ENSP00000360124.4:p.Ile127=
ENST00000371084.7:c.327T>C ENSP00000360125.3:p.Ile109=
ENST00000540265.5:c.-265T>C ENSP00000443449.1:n.-265T>C
ENST00000650546.1:c.327T>C ENSP00000497812.1:p.Ile109=