Canonical Allele Identifier: CA409437528
Gene: PCK1 HGNC NCBI

Linked Data

dbSNP Id: rs2146531087
MyVariant Identifiers: chr20:g.56140590C>A (hg19) chr20:g.57565534C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565534C>A , CM000682.2:g.57565534C>A GRCh38
NC_000020.10:g.56140590C>A , CM000682.1:g.56140590C>A GRCh37
NC_000020.9:g.55573996C>A NCBI36
NG_008205.1:g.9454C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1599C>A MANE Select ENSP00000319814.4:p.Asn533Lys
ENST00000319441.5:c.1599C>A ENSP00000319814.4:p.Asn533Lys
ENST00000467047.1:n.4241C>A
NM_002591.3:c.1599C>A NP_002582.3:p.Asn533Lys
XM_011528839.1:c.1203C>A XP_011527141.1:p.Asn401Lys
XM_024451888.1:c.1203C>A XP_024307656.1:p.Asn401Lys
NM_002591.4:c.1599C>A MANE Select NP_002582.3:p.Asn533Lys
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