Canonical Allele Identifier: CA2371896280
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562812C= , CM000682.2:g.57562812C= GRCh38
NC_000020.10:g.56137868C= , CM000682.1:g.56137868C= GRCh37
NC_000020.9:g.55571274C= NCBI36
NG_008205.1:g.6732C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.523C= MANE Select ENSP00000319814.4:p.Arg175=
ENST00000319441.5:c.523C= ENSP00000319814.4:p.Arg175=
ENST00000467047.1:n.1733C=
ENST00000498194.1:n.465C=
NM_002591.3:c.523C= NP_002582.3:p.Arg175=
XM_011528839.1:c.127C= XP_011527141.1:p.Arg43=
XM_024451888.1:c.127C= XP_024307656.1:p.Arg43=
NM_002591.4:c.523C= MANE Select NP_002582.3:p.Arg175=