Canonical Allele Identifier: CA2371896192
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562675C= , CM000682.2:g.57562675C= GRCh38
NC_000020.10:g.56137731C= , CM000682.1:g.56137731C= GRCh37
NC_000020.9:g.55571137C= NCBI36
NG_008205.1:g.6595C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.407-21C= MANE Select ENSP00000319814.4:n.407-21C=
ENST00000319441.5:c.407-21C= ENSP00000319814.4:n.407-21C=
ENST00000467047.1:n.1596C=
ENST00000498194.1:n.328C=
NM_002591.3:c.407-21C= NP_002582.3:n.407-21C=
XM_011528839.1:c.11-21C= XP_011527141.1:n.11-21C=
XM_024451888.1:c.11-21C= XP_024307656.1:n.11-21C=
NM_002591.4:c.407-21C= MANE Select NP_002582.3:n.407-21C=