Canonical Allele Identifier: CA2371896180
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562654_57562657delinsCAAG , CM000682.2:g.57562654_57562657delinsCAAG GRCh38
NC_000020.10:g.56137710_56137713delinsCAAG , CM000682.1:g.56137710_56137713delinsCAAG GRCh37
NC_000020.9:g.55571116_55571119delinsCAAG NCBI36
NG_008205.1:g.6574_6577delinsCAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.407-42_407-39delinsCAAG MANE Select ENSP00000319814.4:n.407-42_407-39delinsCAAG
ENST00000319441.5:c.407-42_407-39delinsCAAG ENSP00000319814.4:n.407-42_407-39delinsCAAG
ENST00000467047.1:n.1575_1578delinsCAAG
ENST00000498194.1:n.307_310delinsCAAG
NM_002591.3:c.407-42_407-39delinsCAAG NP_002582.3:n.407-42_407-39delinsCAAG
XM_011528839.1:c.11-42_11-39delinsCAAG XP_011527141.1:n.11-42_11-39delinsCAAG
XM_024451888.1:c.11-42_11-39delinsCAAG XP_024307656.1:n.11-42_11-39delinsCAAG
NM_002591.4:c.407-42_407-39delinsCAAG MANE Select NP_002582.3:n.407-42_407-39delinsCAAG