Canonical Allele Identifier: CA2371896171
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562640T= , CM000682.2:g.57562640T= GRCh38
NC_000020.10:g.56137696T= , CM000682.1:g.56137696T= GRCh37
NC_000020.9:g.55571102T= NCBI36
NG_008205.1:g.6560T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.407-56T= MANE Select ENSP00000319814.4:n.407-56T=
ENST00000319441.5:c.407-56T= ENSP00000319814.4:n.407-56T=
ENST00000467047.1:n.1561T=
ENST00000498194.1:n.293T=
NM_002591.3:c.407-56T= NP_002582.3:n.407-56T=
XM_011528839.1:c.11-56T= XP_011527141.1:n.11-56T=
XM_024451888.1:c.11-56T= XP_024307656.1:n.11-56T=
NM_002591.4:c.407-56T= MANE Select NP_002582.3:n.407-56T=