Canonical Allele Identifier: CA340638230
Gene: PGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63648540G>T , CM000663.2:g.63648540G>T GRCh38
NC_000001.10:g.64114211G>T , CM000663.1:g.64114211G>T GRCh37
NC_000001.9:g.63886799G>T NCBI36
NG_016966.1:g.60265G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371084.8:c.1168G>T MANE Select ENSP00000360125.3:p.Asp390Tyr
ENST00000650546.1:c.1168G>T ENSP00000497812.1:p.Asp390Tyr
ENST00000371083.4:c.1222G>T ENSP00000360124.4:p.Asp408Tyr
ENST00000371084.7:c.1168G>T ENSP00000360125.3:p.Asp390Tyr
ENST00000540265.5:c.577G>T ENSP00000443449.1:p.Asp193Tyr
NM_001172818.1:c.1222G>T NP_001166289.1:p.Asp408Tyr
NM_001172819.1:c.577G>T NP_001166290.1:p.Asp193Tyr
NM_002633.2:c.1168G>T NP_002624.2:p.Asp390Tyr
NM_002633.3:c.1168G>T MANE Select NP_002624.2:p.Asp390Tyr
NM_001172819.2:c.577G>T NP_001166290.1:p.Asp193Tyr