Canonical Allele Identifier: CA2371896361
Gene: PCK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562946T= , CM000682.2:g.57562946T= GRCh38
NC_000020.10:g.56138002T= , CM000682.1:g.56138002T= GRCh37
NC_000020.9:g.55571408T= NCBI36
NG_008205.1:g.6866T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.610+47T= MANE Select ENSP00000319814.4:n.610+47T=
ENST00000319441.5:c.610+47T= ENSP00000319814.4:n.610+47T=
ENST00000467047.1:n.1867T=
ENST00000470051.1:n.113T=
ENST00000498194.1:n.552+47T=
NM_002591.3:c.610+47T= NP_002582.3:n.610+47T=
XM_011528839.1:c.214+47T= XP_011527141.1:n.214+47T=
XM_024451888.1:c.214+47T= XP_024307656.1:n.214+47T=
NM_002591.4:c.610+47T= MANE Select NP_002582.3:n.610+47T=
Search 100 bp 5'
Search 100 bp 3'