Canonical Allele Identifier: CA418207992

Gene: PGM1

Linked Data

• MyVariant Identifiers: chr1:g.64095209A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63629538A>T , CM000663.2:g.63629538A>T	GRCh38
NC_000001.10:g.64095209A>T , CM000663.1:g.64095209A>T	GRCh37
NC_000001.9:g.63867797A>T	NCBI36
NG_016966.1:g.41263A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371084.8:c.360A>T MANE Select	ENSP00000360125.3:p.Pro120=
ENST00000650546.1:c.360A>T	ENSP00000497812.1:p.Pro120=
ENST00000371083.4:c.414A>T	ENSP00000360124.4:p.Pro138=
ENST00000371084.7:c.360A>T	ENSP00000360125.3:p.Pro120=
ENST00000540265.5:c.-232A>T	ENSP00000443449.1:n.-232A>T
NM_001172818.1:c.414A>T	NP_001166289.1:p.Pro138=
NM_001172819.1:c.-232A>T	NP_001166290.1:n.-232A>T
NM_002633.2:c.360A>T	NP_002624.2:p.Pro120=
NM_002633.3:c.360A>T MANE Select	NP_002624.2:p.Pro120=
NM_001172819.2:c.-232A>T	NP_001166290.1:n.-232A>T