Canonical Allele Identifier: CA2439138649
Gene: PGK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118297A= , CM000685.2:g.78118297A= GRCh38
NC_000023.10:g.77373794A= , CM000685.1:g.77373794A= GRCh37
NC_000023.9:g.77260450A= NCBI36
NG_008862.1:g.19129A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.641+127A= MANE Select ENSP00000362413.4:n.641+127A=
ENST00000644362.1:c.557+127A= ENSP00000496140.1:n.557+127A=
ENST00000373316.4:c.641+127A= ENSP00000362413.4:n.641+127A=
ENST00000491291.1:n.633+127A=
NM_000291.3:c.641+127A= NP_000282.1:n.641+127A=
NM_000291.4:c.641+127A= MANE Select NP_000282.1:n.641+127A=