Canonical Allele Identifier: CA340645556

Gene: PGM1

Linked Data

• MyVariant Identifiers: chr1:g.64095121A>C (hg19) ; chr1:g.63629450A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.63629450A>C , CM000663.2:g.63629450A>C	GRCh38
NC_000001.10:g.64095121A>C , CM000663.1:g.64095121A>C	GRCh37
NC_000001.9:g.63867709A>C	NCBI36
NG_016966.1:g.41175A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371084.8:c.272A>C MANE Select	ENSP00000360125.3:p.Asn91Thr
ENST00000650546.1:c.272A>C	ENSP00000497812.1:p.Asn91Thr
ENST00000371083.4:c.326A>C	ENSP00000360124.4:p.Asn109Thr
ENST00000371084.7:c.272A>C	ENSP00000360125.3:p.Asn91Thr
ENST00000540265.5:c.-320A>C	ENSP00000443449.1:n.-320A>C
NM_001172818.1:c.326A>C	NP_001166289.1:p.Asn109Thr
NM_001172819.1:c.-320A>C	NP_001166290.1:n.-320A>C
NM_002633.2:c.272A>C	NP_002624.2:p.Asn91Thr
NM_002633.3:c.272A>C MANE Select	NP_002624.2:p.Asn91Thr
NM_001172819.2:c.-320A>C	NP_001166290.1:n.-320A>C