Canonical Allele Identifier: CA331585820
Gene: PGK1 HGNC NCBI

Linked Data

dbSNP Id: rs782555469
gnomAD v2: X-77372685-T-TA
gnomAD v3: X-78117188-T-TA
gnomAD v4: X-78117188-T-TA
MyVariant Identifiers: chrX:g.77372685_77372686insA (hg19) chrX:g.78117188_78117189insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78117194dup , CM000685.2:g.78117194dup GRCh38
NC_000023.10:g.77372691dup , CM000685.1:g.77372691dup GRCh37
NC_000023.9:g.77259347dup NCBI36
NG_008862.1:g.18026dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.418-118dup MANE Select ENSP00000362413.4:n.418-118dup
ENST00000644362.1:c.334-118dup ENSP00000496140.1:n.334-118dup
ENST00000373316.4:c.418-118dup ENSP00000362413.4:n.418-118dup
ENST00000491291.1:n.410-118dup
NM_000291.3:c.418-118dup NP_000282.1:n.418-118dup
NM_000291.4:c.418-118dup MANE Select NP_000282.1:n.418-118dup
Search 100 bp 5'
Search 100 bp 3'