Canonical Allele Identifier: CA2371896352
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562933_57562934delinsTA , CM000682.2:g.57562933_57562934delinsTA GRCh38
NC_000020.10:g.56137989_56137990delinsTA , CM000682.1:g.56137989_56137990delinsTA GRCh37
NC_000020.9:g.55571395_55571396delinsTA NCBI36
NG_008205.1:g.6853_6854delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.610+34_610+35delinsTA MANE Select ENSP00000319814.4:n.610+34_610+35delinsTA
ENST00000319441.5:c.610+34_610+35delinsTA ENSP00000319814.4:n.610+34_610+35delinsTA
ENST00000467047.1:n.1854_1855delinsTA
ENST00000470051.1:n.100_101delinsTA
ENST00000498194.1:n.552+34_552+35delinsTA
NM_002591.3:c.610+34_610+35delinsTA NP_002582.3:n.610+34_610+35delinsTA
XM_011528839.1:c.214+34_214+35delinsTA XP_011527141.1:n.214+34_214+35delinsTA
XM_024451888.1:c.214+34_214+35delinsTA XP_024307656.1:n.214+34_214+35delinsTA
NM_002591.4:c.610+34_610+35delinsTA MANE Select NP_002582.3:n.610+34_610+35delinsTA