Canonical Allele Identifier: CA517379886

Gene: PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77373551C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78118054C>G , CM000685.2:g.78118054C>G	GRCh38
NC_000023.10:g.77373551C>G , CM000685.1:g.77373551C>G	GRCh37
NC_000023.9:g.77260207C>G	NCBI36
NG_008862.1:g.18886C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373316.5:c.525C>G MANE Select	ENSP00000362413.4:p.Ser175=
ENST00000644362.1:c.441C>G	ENSP00000496140.1:p.Ser147=
ENST00000373316.4:c.525C>G	ENSP00000362413.4:p.Ser175=
ENST00000491291.1:n.517C>G
NM_000291.3:c.525C>G	NP_000282.1:p.Ser175=
NM_000291.4:c.525C>G MANE Select	NP_000282.1:p.Ser175=