Canonical Allele Identifier: CA2371896398
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562988G= , CM000682.2:g.57562988G= GRCh38
NC_000020.10:g.56138044G= , CM000682.1:g.56138044G= GRCh37
NC_000020.9:g.55571450G= NCBI36
NG_008205.1:g.6908G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.611-40G= MANE Select ENSP00000319814.4:n.611-40G=
ENST00000319441.5:c.611-40G= ENSP00000319814.4:n.611-40G=
ENST00000467047.1:n.1909G=
ENST00000470051.1:n.155G=
ENST00000498194.1:n.553-40G=
NM_002591.3:c.611-40G= NP_002582.3:n.611-40G=
XM_011528839.1:c.215-40G= XP_011527141.1:n.215-40G=
XM_024451888.1:c.215-40G= XP_024307656.1:n.215-40G=
NM_002591.4:c.611-40G= MANE Select NP_002582.3:n.611-40G=