Canonical Allele Identifier: CA2439140552
Gene: PGK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123388G= , CM000685.2:g.78123388G= GRCh38
NC_000023.10:g.77378885G= , CM000685.1:g.77378885G= GRCh37
NC_000023.9:g.77265541G= NCBI36
NG_008862.1:g.24220G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.936+14G= MANE Select ENSP00000362413.4:n.936+14G=
ENST00000644362.1:c.852+14G= ENSP00000496140.1:n.852+14G=
ENST00000373316.4:c.936+14G= ENSP00000362413.4:n.936+14G=
NM_000291.3:c.936+14G= NP_000282.1:n.936+14G=
NM_000291.4:c.936+14G= MANE Select NP_000282.1:n.936+14G=