Canonical Allele Identifier: CA517380047

Gene: PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77373660C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78118163C>T , CM000685.2:g.78118163C>T	GRCh38
NC_000023.10:g.77373660C>T , CM000685.1:g.77373660C>T	GRCh37
NC_000023.9:g.77260316C>T	NCBI36
NG_008862.1:g.18995C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373316.5:c.634C>T MANE Select	ENSP00000362413.4:p.Leu212=
ENST00000644362.1:c.550C>T	ENSP00000496140.1:p.Leu184=
ENST00000373316.4:c.634C>T	ENSP00000362413.4:p.Leu212=
ENST00000491291.1:n.626C>T
NM_000291.3:c.634C>T	NP_000282.1:p.Leu212=
NM_000291.4:c.634C>T MANE Select	NP_000282.1:p.Leu212=