Canonical Allele Identifier: CA511310958
Gene: PCK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.56140434C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565378C>A , CM000682.2:g.57565378C>A GRCh38
NC_000020.10:g.56140434C>A , CM000682.1:g.56140434C>A GRCh37
NC_000020.9:g.55573840C>A NCBI36
NG_008205.1:g.9298C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1443C>A MANE Select ENSP00000319814.4:p.Ala481=
ENST00000319441.5:c.1443C>A ENSP00000319814.4:p.Ala481=
ENST00000467047.1:n.4085C>A
ENST00000485958.1:n.567C>A
NM_002591.3:c.1443C>A NP_002582.3:p.Ala481=
XM_011528839.1:c.1047C>A XP_011527141.1:p.Ala349=
XM_024451888.1:c.1047C>A XP_024307656.1:p.Ala349=
NM_002591.4:c.1443C>A MANE Select NP_002582.3:p.Ala481=
Search 100 bp 5'
Search 100 bp 3'