Canonical Allele Identifier: CA340645479

Gene: PGM1

Linked Data

• MyVariant Identifiers: chr1:g.64095107G>C (hg19) ; chr1:g.63629436G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63629436G>C , CM000663.2:g.63629436G>C	GRCh38
NC_000001.10:g.64095107G>C , CM000663.1:g.64095107G>C	GRCh37
NC_000001.9:g.63867695G>C	NCBI36
NG_016966.1:g.41161G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371084.8:c.258G>C MANE Select	ENSP00000360125.3:p.Leu86Phe
ENST00000650546.1:c.258G>C	ENSP00000497812.1:p.Leu86Phe
ENST00000371083.4:c.312G>C	ENSP00000360124.4:p.Leu104Phe
ENST00000371084.7:c.258G>C	ENSP00000360125.3:p.Leu86Phe
ENST00000540265.5:c.-334G>C	ENSP00000443449.1:n.-334G>C
NM_001172818.1:c.312G>C	NP_001166289.1:p.Leu104Phe
NM_001172819.1:c.-334G>C	NP_001166290.1:n.-334G>C
NM_002633.2:c.258G>C	NP_002624.2:p.Leu86Phe
NM_002633.3:c.258G>C MANE Select	NP_002624.2:p.Leu86Phe
NM_001172819.2:c.-334G>C	NP_001166290.1:n.-334G>C