Canonical Allele Identifier: CA2580101988
Gene: PGK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2001128
ClinVar RCV Id: RCV002810939

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78117302_78117303dup , CM000685.2:g.78117302_78117303dup GRCh38
NC_000023.10:g.77372799_77372800dup , CM000685.1:g.77372799_77372800dup GRCh37
NC_000023.9:g.77259455_77259456dup NCBI36
NG_008862.1:g.18134_18135dup

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.418-10_418-9dup MANE Select ENSP00000362413.4:n.418-10_418-9dup
ENST00000644362.1:c.334-10_334-9dup ENSP00000496140.1:n.334-10_334-9dup
ENST00000373316.4:c.418-10_418-9dup ENSP00000362413.4:n.418-10_418-9dup
ENST00000491291.1:n.410-10_410-9dup
NM_000291.3:c.418-10_418-9dup NP_000282.1:n.418-10_418-9dup
NM_000291.4:c.418-10_418-9dup MANE Select NP_000282.1:n.418-10_418-9dup