Canonical Allele Identifier: CA2371896343
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562921_57562923delinsCAA , CM000682.2:g.57562921_57562923delinsCAA GRCh38
NC_000020.10:g.56137977_56137979delinsCAA , CM000682.1:g.56137977_56137979delinsCAA GRCh37
NC_000020.9:g.55571383_55571385delinsCAA NCBI36
NG_008205.1:g.6841_6843delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.610+22_610+24delinsCAA MANE Select ENSP00000319814.4:n.610+22_610+24delinsCAA
ENST00000319441.5:c.610+22_610+24delinsCAA ENSP00000319814.4:n.610+22_610+24delinsCAA
ENST00000467047.1:n.1842_1844delinsCAA
ENST00000470051.1:n.88_90delinsCAA
ENST00000498194.1:n.552+22_552+24delinsCAA
NM_002591.3:c.610+22_610+24delinsCAA NP_002582.3:n.610+22_610+24delinsCAA
XM_011528839.1:c.214+22_214+24delinsCAA XP_011527141.1:n.214+22_214+24delinsCAA
XM_024451888.1:c.214+22_214+24delinsCAA XP_024307656.1:n.214+22_214+24delinsCAA
NM_002591.4:c.610+22_610+24delinsCAA MANE Select NP_002582.3:n.610+22_610+24delinsCAA