Canonical Allele Identifier: CA340638458

Gene: PGM1

Linked Data

• MyVariant Identifiers: chr1:g.64114312T>A (hg19) ; chr1:g.63648641T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63648641T>A , CM000663.2:g.63648641T>A	GRCh38
NC_000001.10:g.64114312T>A , CM000663.1:g.64114312T>A	GRCh37
NC_000001.9:g.63886900T>A	NCBI36
NG_016966.1:g.60366T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371084.8:c.1269T>A MANE Select	ENSP00000360125.3:p.Asn423Lys
ENST00000650546.1:c.1269T>A	ENSP00000497812.1:p.Asn423Lys
ENST00000371083.4:c.1323T>A	ENSP00000360124.4:p.Asn441Lys
ENST00000371084.7:c.1269T>A	ENSP00000360125.3:p.Asn423Lys
ENST00000540265.5:c.678T>A	ENSP00000443449.1:p.Asn226Lys
NM_001172818.1:c.1323T>A	NP_001166289.1:p.Asn441Lys
NM_001172819.1:c.678T>A	NP_001166290.1:p.Asn226Lys
NM_002633.2:c.1269T>A	NP_002624.2:p.Asn423Lys
NM_002633.3:c.1269T>A MANE Select	NP_002624.2:p.Asn423Lys
NM_001172819.2:c.678T>A	NP_001166290.1:p.Asn226Lys