Canonical Allele Identifier: CA418208194

Gene: PGM1

Linked Data

• dbSNP Id: rs1225142927
• gnomAD v2: 1-64095254-T-C
• gnomAD v4: 1-63629583-T-C
• MyVariant Identifiers: chr1:g.64095254T>C (hg19) ; chr1:g.63629583T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63629583T>C , CM000663.2:g.63629583T>C	GRCh38
NC_000001.10:g.64095254T>C , CM000663.1:g.64095254T>C	GRCh37
NC_000001.9:g.63867842T>C	NCBI36
NG_016966.1:g.41308T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371084.8:c.405T>C MANE Select	ENSP00000360125.3:p.Asn135=
ENST00000650546.1:c.405T>C	ENSP00000497812.1:p.Asn135=
ENST00000371083.4:c.459T>C	ENSP00000360124.4:p.Asn153=
ENST00000371084.7:c.405T>C	ENSP00000360125.3:p.Asn135=
ENST00000540265.5:c.-187T>C	ENSP00000443449.1:n.-187T>C
NM_001172818.1:c.459T>C	NP_001166289.1:p.Asn153=
NM_001172819.1:c.-187T>C	NP_001166290.1:n.-187T>C
NM_002633.2:c.405T>C	NP_002624.2:p.Asn135=
NM_002633.3:c.405T>C MANE Select	NP_002624.2:p.Asn135=
NM_001172819.2:c.-187T>C	NP_001166290.1:n.-187T>C