Canonical Allele Identifier: CA413717279
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77380389G>T (hg19) chrX:g.78124892G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78124892G>T , CM000685.2:g.78124892G>T GRCh38
NC_000023.10:g.77380389G>T , CM000685.1:g.77380389G>T GRCh37
NC_000023.9:g.77267045G>T NCBI36
NG_008862.1:g.25724G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373316.5:c.955G>T MANE Select ENSP00000362413.4:p.Glu319Ter
ENST00000644362.1:c.871G>T ENSP00000496140.1:p.Glu291Ter
ENST00000373316.4:c.955G>T ENSP00000362413.4:p.Glu319Ter
NM_000291.3:c.955G>T NP_000282.1:p.Glu319Ter
NM_000291.4:c.955G>T MANE Select NP_000282.1:p.Glu319Ter
Search 100 bp 5'
Search 100 bp 3'