Canonical Allele Identifier: CA517473348
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77369355C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78113858C>A , CM000685.2:g.78113858C>A GRCh38
NC_000023.10:g.77369355C>A , CM000685.1:g.77369355C>A GRCh37
NC_000023.9:g.77256011C>A NCBI36
NG_008862.1:g.14690C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.231C>A MANE Select ENSP00000362413.4:p.Ser77=
ENST00000644362.1:c.147C>A ENSP00000496140.1:p.Ser49=
ENST00000373316.4:c.231C>A ENSP00000362413.4:p.Ser77=
ENST00000491291.1:n.223C>A
NM_000291.3:c.231C>A NP_000282.1:p.Ser77=
NM_000291.4:c.231C>A MANE Select NP_000282.1:p.Ser77=
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