Canonical Allele Identifier: CA418207832
Gene: PGM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.64095173C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63629502C>A , CM000663.2:g.63629502C>A GRCh38
NC_000001.10:g.64095173C>A , CM000663.1:g.64095173C>A GRCh37
NC_000001.9:g.63867761C>A NCBI36
NG_016966.1:g.41227C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.324C>A MANE Select ENSP00000360125.3:p.Ala108=
ENST00000650546.1:c.324C>A ENSP00000497812.1:p.Ala108=
ENST00000371083.4:c.378C>A ENSP00000360124.4:p.Ala126=
ENST00000371084.7:c.324C>A ENSP00000360125.3:p.Ala108=
ENST00000540265.5:c.-268C>A ENSP00000443449.1:n.-268C>A
NM_001172818.1:c.378C>A NP_001166289.1:p.Ala126=
NM_001172819.1:c.-268C>A NP_001166290.1:n.-268C>A
NM_002633.2:c.324C>A NP_002624.2:p.Ala108=
NM_002633.3:c.324C>A MANE Select NP_002624.2:p.Ala108=
NM_001172819.2:c.-268C>A NP_001166290.1:n.-268C>A
Search 100 bp 5'
Search 100 bp 3'