Canonical Allele Identifier: CA340645753
Gene: PGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63629486T>C , CM000663.2:g.63629486T>C GRCh38
NC_000001.10:g.64095157T>C , CM000663.1:g.64095157T>C GRCh37
NC_000001.9:g.63867745T>C NCBI36
NG_016966.1:g.41211T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.308T>C MANE Select ENSP00000360125.3:p.Ile103Thr
ENST00000650546.1:c.308T>C ENSP00000497812.1:p.Ile103Thr
ENST00000371083.4:c.362T>C ENSP00000360124.4:p.Ile121Thr
ENST00000371084.7:c.308T>C ENSP00000360125.3:p.Ile103Thr
ENST00000540265.5:c.-284T>C ENSP00000443449.1:n.-284T>C
NM_001172818.1:c.362T>C NP_001166289.1:p.Ile121Thr
NM_001172819.1:c.-284T>C NP_001166290.1:n.-284T>C
NM_002633.2:c.308T>C NP_002624.2:p.Ile103Thr
NM_002633.3:c.308T>C MANE Select NP_002624.2:p.Ile103Thr
NM_001172819.2:c.-284T>C NP_001166290.1:n.-284T>C