Canonical Allele Identifier: CA2371897585
Gene: PCK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565470T= , CM000682.2:g.57565470T= GRCh38
NC_000020.10:g.56140526T= , CM000682.1:g.56140526T= GRCh37
NC_000020.9:g.55573932T= NCBI36
NG_008205.1:g.9390T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1535T= MANE Select ENSP00000319814.4:p.Phe512=
ENST00000319441.5:c.1535T= ENSP00000319814.4:p.Phe512=
ENST00000467047.1:n.4177T=
NM_002591.3:c.1535T= NP_002582.3:p.Phe512=
XM_011528839.1:c.1139T= XP_011527141.1:p.Phe380=
XM_024451888.1:c.1139T= XP_024307656.1:p.Phe380=
NM_002591.4:c.1535T= MANE Select NP_002582.3:p.Phe512=
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