Canonical Allele Identifier: CA340638436
Gene: PGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63648630T>A , CM000663.2:g.63648630T>A GRCh38
NC_000001.10:g.64114301T>A , CM000663.1:g.64114301T>A GRCh37
NC_000001.9:g.63886889T>A NCBI36
NG_016966.1:g.60355T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371084.8:c.1258T>A MANE Select ENSP00000360125.3:p.Tyr420Asn
ENST00000650546.1:c.1258T>A ENSP00000497812.1:p.Tyr420Asn
ENST00000371083.4:c.1312T>A ENSP00000360124.4:p.Tyr438Asn
ENST00000371084.7:c.1258T>A ENSP00000360125.3:p.Tyr420Asn
ENST00000540265.5:c.667T>A ENSP00000443449.1:p.Tyr223Asn
NM_001172818.1:c.1312T>A NP_001166289.1:p.Tyr438Asn
NM_001172819.1:c.667T>A NP_001166290.1:p.Tyr223Asn
NM_002633.2:c.1258T>A NP_002624.2:p.Tyr420Asn
NM_002633.3:c.1258T>A MANE Select NP_002624.2:p.Tyr420Asn
NM_001172819.2:c.667T>A NP_001166290.1:p.Tyr223Asn