Canonical Allele Identifier: CA340638578

Gene: PGM1

Linked Data

• MyVariant Identifiers: chr1:g.64117374A>T (hg19) ; chr1:g.63651703A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63651703A>T , CM000663.2:g.63651703A>T	GRCh38
NC_000001.10:g.64117374A>T , CM000663.1:g.64117374A>T	GRCh37
NC_000001.9:g.63889962A>T	NCBI36
NG_016966.1:g.63428A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371084.8:c.1315A>T MANE Select	ENSP00000360125.3:p.Asn439Tyr
ENST00000650546.1:c.1315A>T	ENSP00000497812.1:p.Asn439Tyr
ENST00000371083.4:c.1369A>T	ENSP00000360124.4:p.Asn457Tyr
ENST00000371084.7:c.1315A>T	ENSP00000360125.3:p.Asn439Tyr
ENST00000483707.1:n.349A>T
ENST00000540265.5:c.724A>T	ENSP00000443449.1:p.Asn242Tyr
NM_001172818.1:c.1369A>T	NP_001166289.1:p.Asn457Tyr
NM_001172819.1:c.724A>T	NP_001166290.1:p.Asn242Tyr
NM_002633.2:c.1315A>T	NP_002624.2:p.Asn439Tyr
NM_002633.3:c.1315A>T MANE Select	NP_002624.2:p.Asn439Tyr
NM_001172819.2:c.724A>T	NP_001166290.1:p.Asn242Tyr