Canonical Allele Identifier: CA418208033

Gene: PGM1

Linked Data

• MyVariant Identifiers: chr1:g.64095218C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63629547C>G , CM000663.2:g.63629547C>G	GRCh38
NC_000001.10:g.64095218C>G , CM000663.1:g.64095218C>G	GRCh37
NC_000001.9:g.63867806C>G	NCBI36
NG_016966.1:g.41272C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371084.8:c.369C>G MANE Select	ENSP00000360125.3:p.Pro123=
ENST00000650546.1:c.369C>G	ENSP00000497812.1:p.Pro123=
ENST00000371083.4:c.423C>G	ENSP00000360124.4:p.Pro141=
ENST00000371084.7:c.369C>G	ENSP00000360125.3:p.Pro123=
ENST00000540265.5:c.-223C>G	ENSP00000443449.1:n.-223C>G
NM_001172818.1:c.423C>G	NP_001166289.1:p.Pro141=
NM_001172819.1:c.-223C>G	NP_001166290.1:n.-223C>G
NM_002633.2:c.369C>G	NP_002624.2:p.Pro123=
NM_002633.3:c.369C>G MANE Select	NP_002624.2:p.Pro123=
NM_001172819.2:c.-223C>G	NP_001166290.1:n.-223C>G