Canonical Allele Identifier: CA2439138629
Gene: PGK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118225C= , CM000685.2:g.78118225C= GRCh38
NC_000023.10:g.77373722C= , CM000685.1:g.77373722C= GRCh37
NC_000023.9:g.77260378C= NCBI36
NG_008862.1:g.19057C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.641+55C= MANE Select ENSP00000362413.4:n.641+55C=
ENST00000644362.1:c.557+55C= ENSP00000496140.1:n.557+55C=
ENST00000373316.4:c.641+55C= ENSP00000362413.4:n.641+55C=
ENST00000491291.1:n.633+55C=
NM_000291.3:c.641+55C= NP_000282.1:n.641+55C=
NM_000291.4:c.641+55C= MANE Select NP_000282.1:n.641+55C=