Canonical Allele Identifier: CA340645472

Gene: PGM1

Linked Data

• dbSNP Id: rs1649128928
• MyVariant Identifiers: chr1:g.64095105T>G (hg19) ; chr1:g.63629434T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63629434T>G , CM000663.2:g.63629434T>G	GRCh38
NC_000001.10:g.64095105T>G , CM000663.1:g.64095105T>G	GRCh37
NC_000001.9:g.63867693T>G	NCBI36
NG_016966.1:g.41159T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371084.8:c.256T>G MANE Select	ENSP00000360125.3:p.Leu86Val
ENST00000650546.1:c.256T>G	ENSP00000497812.1:p.Leu86Val
ENST00000371083.4:c.310T>G	ENSP00000360124.4:p.Leu104Val
ENST00000371084.7:c.256T>G	ENSP00000360125.3:p.Leu86Val
ENST00000540265.5:c.-336T>G	ENSP00000443449.1:n.-336T>G
NM_001172818.1:c.310T>G	NP_001166289.1:p.Leu104Val
NM_001172819.1:c.-336T>G	NP_001166290.1:n.-336T>G
NM_002633.2:c.256T>G	NP_002624.2:p.Leu86Val
NM_002633.3:c.256T>G MANE Select	NP_002624.2:p.Leu86Val
NM_001172819.2:c.-336T>G	NP_001166290.1:n.-336T>G