Canonical Allele Identifier: CA2371896380
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562971C= , CM000682.2:g.57562971C= GRCh38
NC_000020.10:g.56138027C= , CM000682.1:g.56138027C= GRCh37
NC_000020.9:g.55571433C= NCBI36
NG_008205.1:g.6891C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.611-57C= MANE Select ENSP00000319814.4:n.611-57C=
ENST00000319441.5:c.611-57C= ENSP00000319814.4:n.611-57C=
ENST00000467047.1:n.1892C=
ENST00000470051.1:n.138C=
ENST00000498194.1:n.553-57C=
NM_002591.3:c.611-57C= NP_002582.3:n.611-57C=
XM_011528839.1:c.215-57C= XP_011527141.1:n.215-57C=
XM_024451888.1:c.215-57C= XP_024307656.1:n.215-57C=
NM_002591.4:c.611-57C= MANE Select NP_002582.3:n.611-57C=