Canonical Allele Identifier: CA2371896350
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562928C= , CM000682.2:g.57562928C= GRCh38
NC_000020.10:g.56137984C= , CM000682.1:g.56137984C= GRCh37
NC_000020.9:g.55571390C= NCBI36
NG_008205.1:g.6848C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.610+29C= MANE Select ENSP00000319814.4:n.610+29C=
ENST00000319441.5:c.610+29C= ENSP00000319814.4:n.610+29C=
ENST00000467047.1:n.1849C=
ENST00000470051.1:n.95C=
ENST00000498194.1:n.552+29C=
NM_002591.3:c.610+29C= NP_002582.3:n.610+29C=
XM_011528839.1:c.214+29C= XP_011527141.1:n.214+29C=
XM_024451888.1:c.214+29C= XP_024307656.1:n.214+29C=
NM_002591.4:c.610+29C= MANE Select NP_002582.3:n.610+29C=