Canonical Allele Identifier: CA340638455

Gene: PGM1

Linked Data

• MyVariant Identifiers: chr1:g.64114311A>C (hg19) ; chr1:g.63648640A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63648640A>C , CM000663.2:g.63648640A>C	GRCh38
NC_000001.10:g.64114311A>C , CM000663.1:g.64114311A>C	GRCh37
NC_000001.9:g.63886899A>C	NCBI36
NG_016966.1:g.60365A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371084.8:c.1268A>C MANE Select	ENSP00000360125.3:p.Asn423Thr
ENST00000650546.1:c.1268A>C	ENSP00000497812.1:p.Asn423Thr
ENST00000371083.4:c.1322A>C	ENSP00000360124.4:p.Asn441Thr
ENST00000371084.7:c.1268A>C	ENSP00000360125.3:p.Asn423Thr
ENST00000540265.5:c.677A>C	ENSP00000443449.1:p.Asn226Thr
NM_001172818.1:c.1322A>C	NP_001166289.1:p.Asn441Thr
NM_001172819.1:c.677A>C	NP_001166290.1:p.Asn226Thr
NM_002633.2:c.1268A>C	NP_002624.2:p.Asn423Thr
NM_002633.3:c.1268A>C MANE Select	NP_002624.2:p.Asn423Thr
NM_001172819.2:c.677A>C	NP_001166290.1:p.Asn226Thr