Canonical Allele Identifier: CA2371896175
Gene: PCK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562644G= , CM000682.2:g.57562644G= GRCh38
NC_000020.10:g.56137700G= , CM000682.1:g.56137700G= GRCh37
NC_000020.9:g.55571106G= NCBI36
NG_008205.1:g.6564G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.407-52G= MANE Select ENSP00000319814.4:n.407-52G=
ENST00000319441.5:c.407-52G= ENSP00000319814.4:n.407-52G=
ENST00000467047.1:n.1565G=
ENST00000498194.1:n.297G=
NM_002591.3:c.407-52G= NP_002582.3:n.407-52G=
XM_011528839.1:c.11-52G= XP_011527141.1:n.11-52G=
XM_024451888.1:c.11-52G= XP_024307656.1:n.11-52G=
NM_002591.4:c.407-52G= MANE Select NP_002582.3:n.407-52G=
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