Canonical Allele Identifier: CA413716500
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77378750A>C (hg19) chrX:g.78123253A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123253A>C , CM000685.2:g.78123253A>C GRCh38
NC_000023.10:g.77378750A>C , CM000685.1:g.77378750A>C GRCh37
NC_000023.9:g.77265406A>C NCBI36
NG_008862.1:g.24085A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.815A>C MANE Select ENSP00000362413.4:p.Lys272Thr
ENST00000644362.1:c.731A>C ENSP00000496140.1:p.Lys244Thr
ENST00000373316.4:c.815A>C ENSP00000362413.4:p.Lys272Thr
ENST00000474281.1:n.222A>C
NM_000291.3:c.815A>C NP_000282.1:p.Lys272Thr
NM_000291.4:c.815A>C MANE Select NP_000282.1:p.Lys272Thr
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