Canonical Allele Identifier: CA413716491
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77378747C>T (hg19) chrX:g.78123250C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123250C>T , CM000685.2:g.78123250C>T GRCh38
NC_000023.10:g.77378747C>T , CM000685.1:g.77378747C>T GRCh37
NC_000023.9:g.77265403C>T NCBI36
NG_008862.1:g.24082C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.812C>T MANE Select ENSP00000362413.4:p.Ser271Phe
ENST00000644362.1:c.728C>T ENSP00000496140.1:p.Ser243Phe
ENST00000373316.4:c.812C>T ENSP00000362413.4:p.Ser271Phe
ENST00000474281.1:n.219C>T
NM_000291.3:c.812C>T NP_000282.1:p.Ser271Phe
NM_000291.4:c.812C>T MANE Select NP_000282.1:p.Ser271Phe
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