Canonical Allele Identifier: CA2579650774
Gene: PGK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118208T>A , CM000685.2:g.78118208T>A GRCh38
NC_000023.10:g.77373705T>A , CM000685.1:g.77373705T>A GRCh37
NC_000023.9:g.77260361T>A NCBI36
NG_008862.1:g.19040T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.641+38T>A MANE Select ENSP00000362413.4:n.641+38T>A
ENST00000644362.1:c.557+38T>A ENSP00000496140.1:n.557+38T>A
ENST00000373316.4:c.641+38T>A ENSP00000362413.4:n.641+38T>A
ENST00000491291.1:n.633+38T>A
NM_000291.3:c.641+38T>A NP_000282.1:n.641+38T>A
NM_000291.4:c.641+38T>A MANE Select NP_000282.1:n.641+38T>A
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