Canonical Allele Identifier: CA642709315
Gene: PGK1 HGNC NCBI

Linked Data

dbSNP Id: rs1557247656
gnomAD v2: X-77373672-G-A
gnomAD v4: X-78118175-G-A
MyVariant Identifiers: chrX:g.77373672G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78118175G>A , CM000685.2:g.78118175G>A GRCh38
NC_000023.10:g.77373672G>A , CM000685.1:g.77373672G>A GRCh37
NC_000023.9:g.77260328G>A NCBI36
NG_008862.1:g.19007G>A

Transcript Alleles

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