Canonical Allele Identifier: CA418207564

Gene: PGM1

Linked Data

• MyVariant Identifiers: chr1:g.64095116A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63629445A>T , CM000663.2:g.63629445A>T	GRCh38
NC_000001.10:g.64095116A>T , CM000663.1:g.64095116A>T	GRCh37
NC_000001.9:g.63867704A>T	NCBI36
NG_016966.1:g.41170A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371084.8:c.267A>T MANE Select	ENSP00000360125.3:p.Gly89=
ENST00000650546.1:c.267A>T	ENSP00000497812.1:p.Gly89=
ENST00000371083.4:c.321A>T	ENSP00000360124.4:p.Gly107=
ENST00000371084.7:c.267A>T	ENSP00000360125.3:p.Gly89=
ENST00000540265.5:c.-325A>T	ENSP00000443449.1:n.-325A>T
NM_001172818.1:c.321A>T	NP_001166289.1:p.Gly107=
NM_001172819.1:c.-325A>T	NP_001166290.1:n.-325A>T
NM_002633.2:c.267A>T	NP_002624.2:p.Gly89=
NM_002633.3:c.267A>T MANE Select	NP_002624.2:p.Gly89=
NM_001172819.2:c.-325A>T	NP_001166290.1:n.-325A>T