Canonical Allele Identifier: CA517379988

Gene: PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77373647C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78118150C>T , CM000685.2:g.78118150C>T	GRCh38
NC_000023.10:g.77373647C>T , CM000685.1:g.77373647C>T	GRCh37
NC_000023.9:g.77260303C>T	NCBI36
NG_008862.1:g.18982C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373316.5:c.621C>T MANE Select	ENSP00000362413.4:p.Pro207=
ENST00000644362.1:c.537C>T	ENSP00000496140.1:p.Pro179=
ENST00000373316.4:c.621C>T	ENSP00000362413.4:p.Pro207=
ENST00000491291.1:n.613C>T
NM_000291.3:c.621C>T	NP_000282.1:p.Pro207=
NM_000291.4:c.621C>T MANE Select	NP_000282.1:p.Pro207=