Canonical Allele Identifier: CA340638220

Gene: PGM1

Linked Data

• MyVariant Identifiers: chr1:g.64114209A>G (hg19) ; chr1:g.63648538A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63648538A>G , CM000663.2:g.63648538A>G	GRCh38
NC_000001.10:g.64114209A>G , CM000663.1:g.64114209A>G	GRCh37
NC_000001.9:g.63886797A>G	NCBI36
NG_016966.1:g.60263A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371084.8:c.1166A>G MANE Select	ENSP00000360125.3:p.Lys389Arg
ENST00000650546.1:c.1166A>G	ENSP00000497812.1:p.Lys389Arg
ENST00000371083.4:c.1220A>G	ENSP00000360124.4:p.Lys407Arg
ENST00000371084.7:c.1166A>G	ENSP00000360125.3:p.Lys389Arg
ENST00000540265.5:c.575A>G	ENSP00000443449.1:p.Lys192Arg
NM_001172818.1:c.1220A>G	NP_001166289.1:p.Lys407Arg
NM_001172819.1:c.575A>G	NP_001166290.1:p.Lys192Arg
NM_002633.2:c.1166A>G	NP_002624.2:p.Lys389Arg
NM_002633.3:c.1166A>G MANE Select	NP_002624.2:p.Lys389Arg
NM_001172819.2:c.575A>G	NP_001166290.1:p.Lys192Arg